AbbVie Contract Manufacturing DMF, CEP, Written Confirmations, FDF, Prices, Patents, Patents & Exclusivities, Dossier, Manufacturer, Licensing, Distributer, Suppliers, News, GMP

Custom Active Pharmaceutical Ingredient

Opthalmics

Topical

Oral Solid Dose

Microbial Fermentation Services

Hot Melt Extrusion

Biologics Development & Drug Substance Manufacturing

Antibody Drug Conjugates (ADC)

Product List 2025

Potent API and Drug Product

Fill-Finish: PreFilled Syringe

Our Impact 2019

AbbVie Global Supply Chain Management

Click the button for full data set

Corporate Video

Biopharmaceutical Contract Manufacturing Facility

Eye Care Ophthalmic Contract Manufacturing Facility

Fill Finish State of The Art Manufacturing Facility

We are AbbVie

Biologics Ballytivnan

Bioresearch Center Overview

Filling Suite

Harvest Setup

Logistics: Shipping Bottles

Microbiology Testing

POD Filter Disassembly

Water for Injection (WFI) Still

Weigh/Dispense

Introducing AbbVie

Our Principles

DATA COMPILATION #PharmaFlow

CDMO Activity Tracker: Novo’s parent buys Catalent for US$ 16.5 bn; Fujifilm, Merck KGaA, Axplora expand capabilities

During the first half (H1) of 2024, the global contract development and manufacturing organization (CDMO) landscape was driven by the escalating demand for complex drug development and manufacturing.With the industry grappling with constantly evolving therapeutic modalities, CDMOs are racing to invest in cutting-edge technologies and infrastructure to meet the growing needs of pharmaceutical and biotech companies.Some of the key players in the CDMO space are Catalent, EUROAPI, Lonza, Axplora, Thermo Fisher, SEQENS, Samsung Biologics, Fujifilm Diosynth Biotechnologies, Quotient Sciences, Famar, LGM Pharma, Veranova, and Evonik. View CDMO Activity Tracker for H1 2024 (Free Excel Available)Novo’s parent buys Catalent for US$ 16.5 bn; Bora, Lonza, Siegfried expand US footprintDuring H1 2024, several European and Asian drugmakers expanded their footprints in the US. In February, Novo Nordisk’s parent company, the Novo Nordisk Foundation, announced the acquisition of Catalent through its investment arm Novo Holdings for US$ 16.5 billion. Novo Holdings plans to sell three of Catalent’s “fill-finish” sites to Novo Nordisk for US$ 11 billion. The deal is expected to allow the Danish drugmaker “to serve significantly more people living with diabetes and obesity,” a company statement said.Taiwan-headquartered Bora Pharmaceuticals forged ahead with its expansion plans in the US market by acquiring Minnesota-based generics manufacturer Upsher-Smith Laboratories. Emergent BioSolutions said it is selling its Maryland facility to an affiliate of Bora. This site in Camden is part of its CDMO, Emergent Bioservices, and offers clinical and commercial non-viral aseptic fill/finish services on four fill lines, including lyophilization, formulation development, and support services.Swiss drugmaker Lonza has agreed to acquire Genentech’s manufacturing facility in California, US, from Roche for US$ 1.2 billion in cash. The site, located in the city of Vacaville, is one of the largest biologics manufacturing facilities in the world by volume.Lonza also launched an artificial intelligence-driven route design technology for choosing the optimal synthetic pathway to manufacture novel APIs.Switzerland’s Siegfried is acquiring a Wisconsin (US)-based CDMO that specializes in early-phase development and manufacturing services from Curia Global to strengthen its capabilities in North America. Siegfried will further develop the site into its North American Siegfried Acceleration Hub for early-phase CDMO services. View CDMO Activity Tracker for H1 2024 (Free Excel Available) Merck Millipore, SK Bioscience lead CGT boom; Fujifilm, Axplora, expand CDMO capabilitiesThe burgeoning field of cell and gene therapies (CGTs) is driving significant investments in CDMOs. CGTs saw considerable deal-making too. Merck KGaA agreed to buy Wisconsin-based Mirus Bio for US$ 600 million. Mirus Bio is a specialist in the development and commercialization of transfection reagents that are used to help introduce genetic material into cells. These reagents play a key role in the production of viral vectors for CGTs.Similarly, South Korea’s SK Bioscience acquired a 60 percent stake in IDT Biologika GmbH for KRW 339 billion (US$ 244 million). IDT Biologika is a 104-year-old German company that ranks among the top 10 vaccine producers in the world.CDMOs are also expanding their capabilities in order to lead innovation for their pharmaceutical partners. Fujifilm Diosynth Biotechnologies is investing US$ 1.2 billion in its large-scale cell culture CDMO business to further expand its end-to-end bio-manufacturing facility in North Carolina, bringing the total investment in the facility to over US$ 3.2 billion. Similarly, Merck KGaA owned MilliporeSigma made its biggest investment in the Asia-Pacific region in March when it invested € 300 million (US$ 327 million) in a new bioprocessing production center in Daejeon, South Korea.German CDMO giant Axplora is investing € 8 million (US$ 8.73 million) to expand capacity for antibody drug conjugate (ADC) payload manufacturing at its Le Mans site in France. Catalent completed upgrades to its capsule filling capabilities of dry powders for inhalation to handle potent drugs at its Boston facility. This now positions Catalent as the CDMO with the largest GMP capacity for capsule spray-dried and carrier-based inhaled powders.LGM Pharma increased its Analytical Testing Services (ATS) by 50 percent with a US$ 2 million investment and introduced new suppository manufacturing capabilities to its CDMO portfolio. Minakem has invested in a new production unit in Montreal, Canada, for steroid APIs. View CDMO Activity Tracker for H1 2024 (Free Excel Available) EUROAPI kicks off four-year sweeping plan; LegoChem partners Samsung Biologics for ADC programSanofi’s spinoff EUROAPI marked 2024 as a “transition year”, setting in motion its Focus-27 plan for profitable growth in the future. The sweeping four-year plan includes a streamlined value-added portfolio focused on highly differentiated and profitable APIs, and a CDMO focused on late-stage and high-value complex small molecules and tides supported by unique technological platforms. The leading French small molecules player signed a five-year collaboration with Ireland’s Priothera wherein EUROAPI will develop and industrialize the manufacturing process of an innovative, complex molecule for blood cancers – mocravimod. The project will be carried out at EUROAPI’s site in Budapest, which is its center of excellence for complex chemistry.South Korea’s CDMO powerhouse Samsung Biologics has partnered LegoChem Biosciences and will provide antibody development and drug substance manufacturing services as a part of LegoChem’s ADC program designed to treat solid tumors. LegoChem aims to submit an investigational new drug application to the US Food and Drug Administration (FDA) in the first half of 2025. Aurigene and Vipergen have joined forces to offer DNA-encoded library (DEL) screening for drug discovery. By combining Aurigene’s drug discovery capabilities with Vipergen’s DEL screening technologies, they seek to create a powerful tool that can quickly test over a billion small-molecule compounds against different disease targets. Dr. Reddy’s Laboratories’ company Aurigene also inaugurated its biologics facility spread across 70,000 square feet.Chinese biotech startup Pleryon is collaborating with France’s SEQENS, a leader in specialty ingredients, to develop and manufacture the former’s lead candidate, an innovative polymer to treat osteoarthritis. Famar is collaborating with Lavipharm and will serve as the contract manufacturer for the latter’s recently added analgesic pharmaceutical products — Lonarid N and Lonalgal. View CDMO Activity Tracker for H1 2024 (Free Excel Available) Our view Key trends observed in H1 2024 include a surge in investments for fill-finish facilities, a growing emphasis on cell and gene therapies, and advancements in ADC manufacturing. With the proliferation of these new classes of drugs, the CDMO space has been rapidly changing in recent years. In the future, the integration of digital technologies, such as AI and automation, will be a key differentiator for CDMOs looking to optimize their operations and accelerate drug development timelines.

Impressions: 3599

Ophthalmic Dealmakers: Novartis, AbbVie forge deals to develop ocular gene therapies

During the Covid-19 pandemic and the concomitant lockdowns, people may have found it difficult to visit eye clinics or hospitals, but globally, ophthalmology has been witnessing a healthy growth. Several factors are contributing to this growth, such as increasing prevalence of eye diseases due to factors like diabetes, rising geriatric population the world over, and disorders linked to increased screen time. As a result, we are seeing several Big Pharma increase their focus on ophthalmology. According to various market studies, the market for ophthalmic drugs is growing at 5.6 to 6.52 percent per annum. The size of the global ophthalmology market was estimated to be US$ 55.28 billion in 2021, and is projected to grow at a compounded annual rate of 6.52 percent to reach US$ 81.05 billion by 2027. In our first ophthalmic review, we look at the major players in the market, significant deals in the recent past, various ocular diseases and conditions, generic and first-time approvals, and future projections. Access the Ophthalmology Newsmakers Dashboard Increasing focus on geographic atrophy The global ophthalmology market is dominated by players such as Novartis, Bausch & Lomb, F. Hoffmann La-Roche, Regeneron Pharmaceuticals, Allergan, Alcon and Japanese drugmaker Santen Pharmaceutical, among others. The top medical conditions in ophthalmology are age-related macular degeneration (AMD) and macular edema, dry eye syndrome, glaucoma, cataract, retinitis pigmentosa and diabetic retinopathy, presbyopia, and uveitis. Topical, local ocular (i.e., subconjunctival, intravitreal, retrobulbar, and intracameral), and systemic delivery are the most frequently used approaches to deliver ocular drugs, though a number of modern ocular delivery systems are gaining popularity. Geographic atrophy (GA), an advanced form of AMD, is a condition that affects the retina, a part of the eye that sends information to the brain to enable sight. GA is a leading cause of blindness, affecting approximately 5 million patients worldwide, with no approved treatment. A significant amount of deals in ophthalmology were triggered by GA. Take the case of Novartis. In November last year, the Swiss drugmaker decided to offload its stake in Roche for US$ 20.7 billion. And the very next month, it acquired UK-based Gyroscope Therapeutics for US$ 1.5 billion. The acquisition will add an investigational, one-time gene therapy for the treatment of GA to Novartis’ portfolio. The therapy, GT005, is currently in phase 2 clinical trials. Gyroscope also has several other retinal diseases-related assets in its pipeline. In October 2020, Novartis had acquired Vedere Bio, which gave the drug behemoth access to two pre-clinical optogenetic AAV gene therapy programs and novel delivery technology for treating inherited retinal dystrophies and GA, among other drug programs. Similarly, in May 2020, Boehringer Ingelheim had collaborated with CDR-Life to develop antibody fragment-based therapeutics for GA. Other companies developing GA products are Apellis Pharmaceuticals-Sobi and Annexon Biosciences. Access the Ophthalmology Newsmakers Dashboard Recent deals in ophthalmology Last year saw AbbVie and Regenxbio collaborate on developing and commercializing RGX-314, a potential one-time gene therapy for the treatment of wet age-related macular degeneration (wet AMD), diabetic retinopathy (DR), and other chronic retinal diseases. RGX-314 is currently being evaluated in patients with wet AMD in a pivotal trial utilizing sub-retinal delivery, and in patients with wet AMD and DR in two separate phase 2 clinical trials utilizing in-office suprachoroidal delivery. Similarly, in December, Lineage Cell Therapeutics entered into an exclusive worldwide collaboration and license agreement with Roche and Genentech for the development and commercialization of a retinal pigment epithelium (RPE) cell therapy for the treatment of ocular disorders, including advanced dry age-related macular degeneration (dry AMD) with GA. The same month, Aerie Pharmaceuticals had announced an exclusive development and commercialization agreement with Santen for Rhopressa/Rhokiinsa (netarsudil ophthalmic solution) and Rocklatan/Roclanda (netarsudil and latanoprost ophthalmic solution). The expanded collaboration includes Europe, Commonwealth of Independent States (CIS) countries, China, India, parts of Latin America and the Oceania countries. In October 2020, Swedish Orphan Biovitrum AB or Sobi and Apellis Pharmaceuticals had announced a strategic collaboration to accelerate the advancement of systemic pegcetacoplan, a targeted C3 therapy for the treatment of multiple rare diseases with high unmet need that impact over 275,000 patients globally. Bausch Health had spun off its eye-care business in August 2020 to unlock value in its iconic brand and its integrated portfolio of eye health products. The spin-off has established two separate companies (a) a pure play eye-health company; and (b) a diversified pharmaceutical company with leading positions in gastroenterology, aesthetics/dermatology, neurology, and international pharmaceuticals. In January this year, Bausch & Lomb announced that it plans to raise US$ 100 million through an initial public offering. Last year, Akorn sold off its consumer health business to an affiliate of Prestige Consumer Healthcare for US$ 230 million. The sell-off included popular over-the-counter ophthalmology drug — TheraTears — besides several other products. Access the Ophthalmology Newsmakers Dashboard FDA approves first generic for Restasis Generic drugs offer cheaper alternatives to patients across the world. This year, ophthalmology saw the biggest generic approval when Mylan Pharmaceuticals, now Viatris, became the first company to bag the US Food and Drug Administration’s nod for Restasis (cyclosporine ophthalmic emulsion). Allergan had transferred patents for the ophthalmic form Restasis to the St. Regis tribe of the Mohawk people in the US to avoid competition. Following the deal, the American drugmaker had received heavy criticism. On February 23, 2018, the US Patent and Trademark Office deemed the Restasis patents invalid and rejected the tribe’s ability to use sovereign immunity to protect the Restasis patents. The other important generic approval was both the FDA and European Medicines Agency’s (EMA) approval of Samsung Bioepis and Biogen’s Byooviz, a biosimilar candidate referencing Lucentis (ranibizumab). While the FDA approval came in September, the EMA nod was given a few months earlier. Byooviz has been approved for the treatment of neovascular wet AMD, visual impairment due to diabetic macular edema (DME), proliferative diabetic retinopathy (PDR), visual impairment due to macular edema, secondary to retinal vein occlusion (branch RVO or central RVO), and visual impairment due to choroidal neovascularization (CNV) in the European Union (EU). Among first-time approvals, FDA approved Allergan’s Vuity (pilocarpine HCl ophthalmic solution) in October last year. This is the first and only eye drop approved by the FDA to treat presbyopia, an age-related blurry near vision. Presbyopia is a common and progressive eye condition that affects 128 million Americans, or nearly half of the adult population in the US. The other important drug that bagged FDA approval this year was Roche’s Vabysmo. The drug targets and inhibits two disease pathways that drive neovascular or wet AMD and DME. Vabysmo is the only injectable eye medicine approved simultaneously in the US for wet AMD and DME, with flexible dosing regimens based on patient needs. Access the Ophthalmology Newsmakers Dashboard Our view Over the last few years, gene therapy, stem cell therapy, and target discovery through genomic research have shown considerable promise as potential strategies to achieve tissue repair or regeneration in the treatment of ocular diseases, such as AMD. At present, a number of gene therapies are undergoing clinical investigations for AMD. Moreover, several modern ocular delivery systems have made significant advances and have proven to be safe and effective. Similarly, artificial retinas, 3D bioprinting and electronic support devices for patients with visual impairments are some promising technologies that will see more growth in the future. According to the World Health Organization (WHO), the aging population is expected to burden all areas of healthcare. Interestingly, ophthalmologists provide approximately 90 percent of their procedure-based services to seniors. Therefore, the market is bound to see healthy growth rates, with newer therapies and ocular delivery systems. Access the Ophthalmology Newsmakers Dashboard

Impressions: 4912

NEWS #PharmaBuzz

Success Factors for Pre-Filled Syringe CMO Selection

15 Jul 2024

// PRESS RELEASE

AbbVie Preps Global Parenteral Sites For Annex 1 Compliance Requirements

24 Jun 2024

// PRESS RELEASE

Translating Environmental, Social and Governance (ESG) Benefits to our Partners

10 May 2024

// PRESS RELEASE

AbbVie Contract Manufacturing – 12-Time CMO Leadership Award Winner

20 Mar 2024

// PRESS RELEASE

AbbVie Contract Manufacturing Recognized by Life Science Leader,11th Year

11 Mar 2024

// PRESS RELEASE

Four Myths About Embedded CMOs, Busted

18 Jan 2024

// PRESS RELEASE

ALL APIs

01

Cyclosporine

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

German Wound Congress

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

USDMF

Click Us!

CEP/COS

JDMF EU-WC NDC

KDMF

VMF Others AUDIT

Product
Web Link

02

Erythromycin

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

German Wound Congress

Not Confirmed

USDMF

CEP/COS

JDMF EU-WC NDC KDMF VMF Others AUDIT

Product
Web Link

03

Erythromycin

U.S.A

Ritonavir

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

German Wound Congress

Not Confirmed

USDMF CEP/COS

JDMF EU-WC NDC KDMF VMF Others AUDIT

Product
Web Link

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

USDMF

01

Butorphanol Tartrate

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 8904

Submission : 1990-12-20

Status : Active

Type : II

Product
Web Link

02

Cyclosporine Usp

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 13800

Submission : 1998-09-01

Status : Active

Type : II

Product
Web Link

03

Erythromycin Base

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 13197

Submission : 1998-04-30

Status : Active

Type : II

Product
Web Link

04

Erythromycin Base

U.S.A

GDUFA

DMF Review : Complete

Rev. Date : 2016-05-09

Pay. Date : 2013-09-25

DMF Number : 27155

Submission : 2015-11-10

Status : Active

Type : II

Product
Web Link

05

Erythromycin Ethylsuccinate

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 13443

Submission : 1998-09-01

Status : Active

Type : II

Product
Web Link

06

Erythromycin Stearate

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 13372

Submission : 1998-09-01

Status : Active

Type : II

Product
Web Link

07

Paricalcitol Drug Substance

U.S.A

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 24315

Submission : 2010-11-30

Status : Active

Type : II

Product
Web Link

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

CEP/COS

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

KDMF

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

NDC API

Only 10 entries up to this point, click to access all

LISTED APIs

01

Biperiden HCl

U.S.A

German Wound Congress

U.S.A

German Wound Congress

Not Confirmed

Stock Recap
#Pipeline Prospector

Product
Web Link

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Drugs in Development

01 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Upadacitinib,Corticosteroid

Therapeutic Area : Immunology

Highest Development Status : Approved FDF

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie Wins EU Nod for RINVOQ in Adults with Giant Cell Arteritis

Details : Rinvoq (upadacitinib) is a FDA approved selective JAK inhibitor that is being investigated in adult patients with giant cell arteritis in a Phase 3 clinical trial.

Product Name : Rinvoq

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

April 08, 2025

02 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Upadacitinib,Corticosteroid

Therapeutic Area : Immunology

Highest Development Status : Phase III

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie gets Positive CHMP Opinion for RINVOQ® in Giant Cell Arteritis Treatment

Details : Rinvoq (upadacitinib) is a FDA approved selective JAK inhibitor that is being investigated in adult patients with giant cell arteritis in a Phase 3 clinical trial.

Product Name : Rinvoq

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

February 28, 2025

03 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Aztreonam,Avibactam,Metronidazole

Therapeutic Area : Infections and Infectious Diseases

Highest Development Status : Approved FDF

Partner/Sponsor/Collaborator : Pfizer Inc

Deal Size : Inapplicable

Deal Type : Inapplicable

U.S. FDA Approves EMBLAVEO™ for Complicated Intra-Abdominal Infections

Details : Emblaveo (aztreonam-avibactam), a beta-lactamase inhibitor, has been FDA approved for the treatment of adult patients with complicated intra-abdominal infections in patients 18 years and older.

Product Name : Emblaveo

Product Type : Antibiotic

Upfront Cash : Inapplicable

February 07, 2025

04 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Epcoritamab,Cyclophosphamide,Rituximab

Therapeutic Area : Oncology

Highest Development Status : Phase III

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

Two Data Analyses Show Epcoritamab Induces Durable Complete Responses

Details : Tepkinly (epcoritamab) is an IgG1-bispecific antibody, which is evaluated for the treatment of diffuse large B-cell lymphoma. It is designed to direct cytotoxic T cells selectively.

Product Name : Tepkinly

Product Type : Antibody

Upfront Cash : Inapplicable

December 09, 2024

05 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Tavapadon

Therapeutic Area : Neurology

Highest Development Status : Phase III

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie Reports Topline Results from Phase 3 TEMPO-2 Trial of Tavapadon in Parkinson’s

Details : CVL-751 (tavapadon) is the first and only D1/D5 receptor partial agonist, which is being studied as a once-daily treatment for patients with parkinson’s disease.

Product Name : CVL-751

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

December 09, 2024

06 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Atogepant

Therapeutic Area : Neurology

Highest Development Status : Phase III

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie Shares Data Supporting Long-Term Efficacy of Atogepant for Preventive Migraine

Details : Qulipta (atogepant) is an orally administered, CGRP receptor antagonist specifically developed for the preventive treatment of chronic and episodic migraine in adults.

Product Name : Qulipta

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

December 04, 2024

07 Immunogen

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Mirvetuximab Soravtansine

Therapeutic Area : Oncology

Highest Development Status : Approved FDF

Partner/Sponsor/Collaborator : AbbVie Inc

Deal Size : $10,100.0 million

Deal Type : Acquisition

AbbVie Completes Acquisition of ImmunoGen

Details : The acquisition accelerates AbbVie's presence in the solid tumor space by adding Elahere (mirvetuximab soravtansine-gynx), an ADC approved for FRα-positive platinum-resistant ovarian cancer.

Product Name : Elahere

Product Type : Antibody-drug Conjugate

Upfront Cash : $10,100.0 million

December 02, 2024

08 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Mirvetuximab Soravtansine

Therapeutic Area : Oncology

Highest Development Status : Approved FDF

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie Secures EU Approval for ELAHERE® in Platinum-Resistant Ovarian Cancer

Details : Elahere (mirvetuximab soravtansine) is a first-in-class antibody-drug conjugate (ADC) approved for folate receptor alpha (FRα) positive platinum-resistant ovarian cancer.

Product Name : Elahere

Product Type : Antibody-drug Conjugate

Upfront Cash : Inapplicable

November 18, 2024

09 AbbVie Inc

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Emraclidine

Therapeutic Area : Psychiatry/Psychology

Highest Development Status : Phase II

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

AbbVie’s $9B Bet Collapses as Closely Watched Schizophrenia Drug Fails Studies

Details : CVL-231 (emraclidine) is a potential novel M4-selective positive allosteric modulator in development for schizophrenia and other psychosis related diseases.

Product Name : CVL-231

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

November 11, 2024

10 Allergan Aesthetics

U.S.A

German Wound Congress

Not Confirmed

Lead Product(s) : Onabotulinumtoxin A

Therapeutic Area : Dermatology

Highest Development Status : Approved FDF

Partner/Sponsor/Collaborator : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

Allergan Launches BOTOX Cosmetic for Masseter Muscle Prominence in China

Details : Botox Cosmetic (onabotulinumtoxinA) is first and only product of its kind that is approved by U.S. FDA to treat Masseter Muscle Prominence in adults.

Product Name : Botox Cosmetic

Product Type : Other Large Molecule

Upfront Cash : Inapplicable

November 09, 2024

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

FDF Dossiers

01

Brand Name : VICODIN HP

U.S.A

Regulatory Info : DISCN

Registration Country : USA

Dosage Form : TABLET;ORAL

Dosage Strength : 660MG;10MG

Packaging :

Approval Date : 1996-09-23

Application Number : 40117

Regulatory Info : DISCN

Registration Country : USA

Product
Web Link

02

Brand Name : VICODIN ES

U.S.A

Regulatory Info : DISCN

Registration Country : USA

Dosage Form : TABLET;ORAL

Dosage Strength : 750MG;7.5MG

Packaging :

Approval Date : 1988-12-09

Application Number : 89736

Regulatory Info : DISCN

Registration Country : USA

Product
Web Link

03

Brand Name : VICODIN

U.S.A

Regulatory Info : DISCN

Registration Country : USA

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG;5MG

Packaging :

Approval Date : 1983-01-07

Application Number : 88058

Regulatory Info : DISCN

Registration Country : USA

Product
Web Link

04

Brand Name : SORIATANE

U.S.A

Regulatory Info : Prescription

Registration Country : Canada

ACITRETIN

Dosage Form : CAPSULE

Dosage Strength : 10MG

Packaging : 30

Approval Date :

Application Number : 2070847

Regulatory Info : Prescription

Registration Country : Canada

Product
Web Link

05

Brand Name : SORIATANE

U.S.A

Regulatory Info : Prescription

Registration Country : Canada

ACITRETIN

Dosage Form : CAPSULE

Dosage Strength : 25MG

Packaging : 30

Approval Date :

Application Number : 2070863

Regulatory Info : Prescription

Registration Country : Canada

Product
Web Link

06

Brand Name : ACYCLOVIR

U.S.A

Regulatory Info : DISCN

Registration Country : USA

ACYCLOVIR SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1999-07-26

Application Number : 75114

Regulatory Info : DISCN

Registration Country : USA

Product
Web Link

07

Brand Name : Humira

U.S.A

Regulatory Info :

Registration Country : Australia

Dosage Form :

Dosage Strength :

Packaging : 2

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Product
Web Link

08

Brand Name : Humira

U.S.A

Regulatory Info :

Registration Country : Australia

Dosage Form :

Dosage Strength :

Packaging : 2

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Product
Web Link

09

Brand Name : Humira

U.S.A

Regulatory Info :

Registration Country : Australia

Dosage Form :

Dosage Strength :

Packaging : 2

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Product
Web Link

10

Brand Name : Humira

U.S.A

Regulatory Info :

Registration Country : Australia

Dosage Form :

Dosage Strength :

Packaging : 2

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Product
Web Link

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

FDA Orange Book

01

Brand Name : VICODIN HP

U.S.A

RLD : No

TE Code :

Dosage Form : TABLET; ORAL

Dosage Strength : 660MG;10MG

Approval Date : 1996-09-23

Application Number : 40117

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

02

Brand Name : VICODIN

U.S.A

RLD : No

TE Code :

Dosage Form : TABLET; ORAL

Dosage Strength : 500MG;5MG

Approval Date : 1983-01-07

Application Number : 88058

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

03

Brand Name : VICODIN ES

U.S.A

RLD : No

TE Code :

Dosage Form : TABLET; ORAL

Dosage Strength : 750MG;7.5MG

Approval Date : 1988-12-09

Application Number : 89736

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

04

Brand Name : ACYCLOVIR

U.S.A

RLD : No

TE Code :

ACYCLOVIR SODIUM

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : EQ 50MG BASE/ML

Approval Date : 1999-07-26

Application Number : 75114

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

05

Brand Name : HUMIRA

U.S.A

RLD :

TE Code :

ADALIMUMAB

Dosage Form : SYRINGE

Dosage Strength : 40MG/0.8ML

Approval Date :

Application Number : 125057

RX/OTC/DISCN :

RLD :

TE Code :

Product
Web Link

06

Brand Name : HUMIRA

U.S.A

RLD :

TE Code :

ADALIMUMAB

Dosage Form : VIAL

Dosage Strength : 40MG/0.8ML

Approval Date :

Application Number : 125057

RX/OTC/DISCN :

RLD :

TE Code :

Product
Web Link

07

Brand Name : LASTACAFT

U.S.A

RLD : Yes

TE Code :

ALCAFTADINE

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Dosage Strength : 0.25%

Approval Date : 2010-07-28

Application Number : 22134

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

Product
Web Link

08

Brand Name : SAPHRIS

U.S.A

RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Dosage Form : TABLET; SUBLINGUAL

Dosage Strength : EQ 5MG BASE

Approval Date : 2009-08-13

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
Web Link

09

Brand Name : SAPHRIS

U.S.A

RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Dosage Form : TABLET; SUBLINGUAL

Dosage Strength : EQ 10MG BASE

Approval Date : 2009-08-13

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
Web Link

10

Brand Name : SAPHRIS

U.S.A

RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Dosage Form : TABLET; SUBLINGUAL

Dosage Strength : EQ 2.5MG BASE

Approval Date : 2015-03-12

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
Web Link

Only 10 entries up to this point, click to access all

Europe

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Canada

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Australia

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

South Africa

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Services

Discover the service capabilities from this company

API Manufacturing

Discover their expertise for :

Contract Manufacturing

01

API CONTRACT MANUFACTURING

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

AbbVie CMO has leveraged its scientific and manufacturing expertise to deliver custom active pharmaceutical ingredients (APIs) across 2 sites in the US and Europe.

Category : Contract Manufacturing

Sub Category : Overview

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

API CONTRACT MANUFACTURING

AbbVie CMO has leveraged its scientific and manufacturing expertise to deliver custom active pharmaceutical ingredients (APIs) across 2 sites in the US and Europe.

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Antibody Drug Conjugate

01

ADC CONTRACT MANUFACTURING

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

AbbVie CMO has expertise in late-stage scale-up and ADC contract manufacturing, coordinating either individual or collective elements of the complex ADC supply chain, from antibody intermediate to conjugation and final fill finish.

Category : Antibody Drug Conjugate

Sub Category : Overview

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

ADC CONTRACT MANUFACTURING

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

High Potency APIs (HPAPIs)

01

MANUFACTURING OF HIGHLY POTENT A...

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

AbbVie CMO has the capability of producing HPAPI with containment capabilities up to OEB5 (<0.1 µg/m3). Its Campoverde and Sligo sites have over 20 years of experience and can support a broad range of commercial GMP batch sizes from gram scale to 600 kg.

Category : High Potency APIs (HPAPIs)

Sub Category : Overview

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : API Manufacturing

MANUFACTURING OF HIGHLY POTENT APIs

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Biologics, Bioprocess & Fermentation

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Drug Product Manufacturing

Discover their expertise for :

Gel

01

TOPICAL GEL CONTRACT MANUFACTURI...

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Drug Product Manufacturing

AbbVie Contract Manufacturing offers topical filling services in Waco, Texas. It offers manufacturing services for various dosage forms, including topical gels and creams.

Category : Gel

Sub Category : Overview

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Drug Product Manufacturing

TOPICAL GEL CONTRACT MANUFACTURING

AbbVie Contract Manufacturing offers topical filling services in Waco, Texas. It offers manufacturing services for various dosage forms, including topical gels and creams.

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Liquid

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Tablet

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Capsule

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Solution

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Biologic Drugs

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Lyophilization

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Cream / Lotion / Ointment

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Technologies

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Injectable / Parenteral

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

API & Drug Product Development

Discover their expertise for :

Preformulation & Material Science

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Formulation Development

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Packaging

Discover their expertise for :

Contract Services

01

CONTRACT PACKAGING SERVICES

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Packaging

AbbVie offers end-to-end manufacturing, from API to bulk oral solid dose to finished drug product packaging. Its packaging types include blisters, bottles, tubes, sachets and sticks, syringes, etc.

Category : Contract Services

Sub Category : Overview

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Packaging

CONTRACT PACKAGING SERVICES

AbbVie offers end-to-end manufacturing, from API to bulk oral solid dose to finished drug product packaging. Its packaging types include blisters, bottles, tubes, sachets and sticks, syringes, etc.

02

PREFILLED SYRINGE (PFS) PACKAGIN...

U.S.A

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Packaging

AbbVie's reputation for quality control, compliance and operational excellence helps it complete the manufacturing process by filling products into sterile syringes or vials. It also offers prefilled syringe (PFS) manufacturing and packaging services.

Category : Contract Services

Sub Category : Pre-Filled Syringe

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

Pharma Service : Packaging

PREFILLED SYRINGE (PFS) PACKAGING

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

KEY SERVICES

TOP RANKED SUPPLIER FOR:

Topical Formulation Development Services

Prefilled Syringe Contract Manufacturing

Inspections and registrations

Check the inspections & registration from this company

FDA

01 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2024-06-18

City : North Chicago

State : Illinois

Country/Area : US

Zip : 60064

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2024-06-18

Product
Web Link

02 FDA Audited

USA

District Decision : No Action Indicated

Inspection End Date : 2024-04-19

City : North Chicago

State : Illinois

Country/Area : US

Zip : 60064

District :

Center :

Project Area : Bioresearch Monitoring

District Decision : No Action Indicated

Inspection End Date : 2024-04-19

Product
Web Link

03 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2024-04-18

City : Barceloneta

State : Puerto Rico

Country/Area : US

Zip : 00617

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2024-04-18

Product
Web Link

04 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-10-30

City : Barceloneta

State : Puerto Rico

Country/Area : US

Zip : 00617

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-10-30

Product
Web Link

05 FDA Audited

USA

District Decision : No Action Indicated

Inspection End Date : 2023-05-12

City : Wyandotte

State : Michigan

Country/Area : US

Zip : 48192

District :

Center :

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2023-05-12

Product
Web Link

06 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-01-31

City : North Chicago

State : Illinois

Country/Area : US

Zip : 60064

District :

Center :

Project Area : Monitoring of Marketed Animal Dr...

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-01-31

Product
Web Link

07 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-01-31

City : North Chicago

State : Illinois

Country/Area : US

Zip : 60064

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-01-31

Product
Web Link

08 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2022-12-14

City : Sligo

State : -

Country/Area : IE

Zip : -

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2022-12-14

Product
Web Link

09 FDA Audited

USA

District Decision : No Action Indicated

Inspection End Date : 2022-10-06

City : North Chicago

State : Illinois

Country/Area : US

Zip : 60064

District :

Center :

Project Area : Bioresearch Monitoring

District Decision : No Action Indicated

Inspection End Date : 2022-10-06

Product
Web Link

10 FDA Audited

USA

District Decision : Voluntary Action Indicated

Inspection End Date : 2022-05-20

City : Aprilia

State : -

Country/Area : IT

Zip : -

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2022-05-20

Product
Web Link

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

EDQM

01

GMP Certified

Type : GMP Certificates

Number : 35424/M0014...

EudraGMDP Key : 175650

Country : Ireland

Issue Date : 2025-02-19

Post Code :

NCA Ref : 164546262339...

City : Westport

Product
Web Link

02

GMP Certified

Type : GMP Certificates

Number : IT/15/H/202...

EudraGMDP Key : 175596

Country : Italy

Issue Date : 2025-02-13

Post Code :

NCA Ref : 000000100069

City : Campoverde Di Aprilia

Product
Web Link

03

GMP Certified

Type : GMP Certificates

Number : IT/15/H/202...

EudraGMDP Key : 175597

Country : Italy

Issue Date : 2025-02-13

Post Code :

NCA Ref : 000000100069

City : Campoverde Di Aprilia

Product
Web Link

04

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 175451

Country : Germany

Issue Date : 2025-02-04

Post Code :

NCA Ref : 00017388

City : Ludwigshafen Am Rhein

Product
Web Link

05

GMP Certified

Type : GMP Certificates

Number : NL/H 24/205...

EudraGMDP Key : 175251

Country : Netherlands

Issue Date : 2025-01-30

Post Code :

NCA Ref : 170843284557...

City : Zwolle

Product
Web Link

06

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 175119

Country : Germany

Issue Date : 2025-01-07

Post Code :

NCA Ref : 00017388

City : Ludwigshafen Am Rhein

Product
Web Link

07

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 173860

Country : U.S.A

Issue Date : 2024-11-20

Post Code :

NCA Ref : 173249848198...

City : North Chicago

Product
Web Link

08

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 173950

Country : U.S.A

Issue Date : 2024-11-20

Post Code :

NCA Ref : 173249848198...

City : North Chicago

Product
Web Link

09

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 173995

Country : U.S.A

Issue Date : 2024-11-20

Post Code :

NCA Ref : 173249848198...

City : North Chicago

Product
Web Link

10

GMP Certified

Type : GMP Certificates

Number : DE_RP_01_GM...

EudraGMDP Key : 174032

Country : U.S.A

Issue Date : 2024-11-20

Post Code :

NCA Ref : 173249848198...

City : North Chicago

Product
Web Link

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

GDUFA

01 GDUFA fees paid

USA

German Wound Congress

Not Confirmed

Paid in : 2025

API Manufacturer :

FDF Manufacturer : FDF MANUFACTURE

Facility Name : AbbVie INC

Business Address : 1N Waukegan Road North Chica...

FEI Number : 3009751352

Country : U.S.A

Paid in : 2025

Product
Web Link

02 GDUFA fees paid

USA

German Wound Congress

Not Confirmed

Paid in : 2025

API Manufacturer : API MANUFACTURE

FDF Manufacturer :

Facility Name : AbbVie INC

Business Address : 1401 Sheridan Road North Chi...

FEI Number : 1411365

Country : U.S.A

Paid in : 2025

Product
Web Link

03 GDUFA fees paid

USA

German Wound Congress

Not Confirmed

Paid in : 2025

API Manufacturer :

FDF Manufacturer : FDF MANUFACTURE

Facility Name : Allergan Pharmaceuticals Irela...

Business Address : Castlebar Road Westport Coun...

FEI Number : 3002806285

Country : U.S.A

Paid in : 2025

Product
Web Link

04 GDUFA fees paid

USA

German Wound Congress

Not Confirmed

Paid in : 2025

API Manufacturer :

FDF Manufacturer : FDF MANUFACTURE

Facility Name : Allergan Sales LLC

Business Address : 8301 Mars Drive Waco TX 7671...

FEI Number : 1643525

Country : U.S.A

Paid in : 2025

Product
Web Link