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07-09 January, 2025
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INTERVIEW #SpeakPharma
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08 Jan 2025
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/us-fda-confirms-class-1-resubmission-of-the-supplemental-new-drug-application-for-izervay-avacincaptad-pegol-intravitreal-solution-for-geographic-atrophy-302346418.html
08 Jan 2025
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/chinas-national-medical-products-administration-nmpa-approves-padcev-in-combination-with-keytruda-pembrolizumab-for-the-treatment-of-advanced-bladder-cancer-302345641.html
24 Dec 2024
// FDA
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/astellas-pharma-us-inc-issues-voluntary-nationwide-recall-one-lot-prografr-05mg-tacrolimus-and-one
19 Dec 2024
// FIERCE BIOTECH
https://www.fiercebiotech.com/biotech/astellas-pays-sangamo-20m-upfront-improve-neurological-gene-therapy-capabilities
19 Dec 2024
// BUSINESSWIRE
19 Dec 2024
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/astellas-and-sangamo-therapeutics-announce-capsid-license-agreement-to-deliver-genomic-medicines-for-neurological-diseases-302335494.html
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16833
Submission : 2003-09-12
Status : Active
Type : II
Registration Number : 217MF11288
Registrant's Address : 2-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-22
Latest Date of Registration :
Registrant Name : Astellas Pharma Korea Co., Ltd.
Registration Date : 2012-08-07
Registration Number : 20120807-204-I-74-02
Manufacturer Name : Astellas Pharma Inc. Toyama Technology Center
Manufacturer Address : 2-178 Kojin-machi, Toyama city, Toyama 930-0809, Japan
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11761
Submission : 1995-12-01
Status : Inactive
Type : II
Certificate Number : CEP 2007-253 - Rev 05
Issue Date : 2024-10-24
Type : Chemical
Substance Number : 2131
Status : Valid
NDC Package Code : 12838-2788
Start Marketing Date : 2010-07-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Astellas Pharma Korea Co., Ltd.
Registration Date : 2023-07-06
Registration Number : 20230706-209-J-1474
Manufacturer Name : Astellas Ireland Co. Limited
Manufacturer Address : Damastown Road, Damastown Industrial Park, Dublin 15, D15 K851, Ireland
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9478
Submission : 1991-12-31
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-073 - Rev 00
Issue Date : 2006-07-13
Type : TSE
Substance Number : 1188
Status : Withdrawn by Holder
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7356
Submission : 1988-02-29
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12856
Submission : 1998-02-11
Status : Active
Type : II
Registrant Name : Astellas Pharma Korea Co., Ltd.
Registration Date : 2006-05-11
Registration Number : Number 118-1-ND
Manufacturer Name : Astellas Pharma Inc. Toyama Technology Center
Manufacturer Address : 2-178, Kojin-machi, Toyama-city, Toyama 930-0809, Japan (3-11, Nihenbashi-honcho 2chome, Chuo-ku, Tokyo 103-8411, Japan)
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10156
Submission : 1991-10-08
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12380
Submission : 1997-02-24
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10769
Submission : 1994-03-14
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10116
Submission : 1993-03-03
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1054
Submission : 1967-04-21
Status : Inactive
Type : II
Details:
Under the license agreement, Astellas will leverage Sangamo's novel proprietary neurotropic adeno-associated virus (AAV) capsid, STAC-BBB for the treatment of neurological diseases.
Lead Product(s): AAV based Gene Therapy
Therapeutic Area: Neurology Brand Name: Undisclosed
Study Phase: Discovery PlatformProduct Type: Cell and Gene therapy
Recipient: Sangamo Therapeutics
Deal Size: $1,320.0 million Upfront Cash: $20.0 million
Deal Type: Licensing Agreement December 19, 2024
Lead Product(s) : AAV based Gene Therapy
Therapeutic Area : Neurology
Highest Development Status : Discovery Platform
Recipient : Sangamo Therapeutics
Deal Size : $1,320.0 million
Deal Type : Licensing Agreement
Astellas, Sangamo Partner on Genomic Medicines for Neurological Disease Via Capsid Tech
Details : Under the license agreement, Astellas will leverage Sangamo's novel proprietary neurotropic adeno-associated virus (AAV) capsid, STAC-BBB for the treatment of neurological diseases.
Brand Name : Undisclosed
Molecule Type : Cell and Gene therapy
Upfront Cash : $20.0 million
December 19, 2024
Details:
IZERVAY (avacincaptad pegol intravitreal solution), a complement C5 inhibitor for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Lead Product(s): Avacincaptad Pegol
Therapeutic Area: Ophthalmology Brand Name: Izervay
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 19, 2024
Lead Product(s) : Avacincaptad Pegol
Therapeutic Area : Ophthalmology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
FDA Rejects Astellas’ Effort to Support Longer Use of Eye Drug Izervay
Details : IZERVAY (avacincaptad pegol intravitreal solution), a complement C5 inhibitor for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Brand Name : Izervay
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 19, 2024
Details:
Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area: Oncology Brand Name: Vyloy
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 21, 2024
Lead Product(s) : Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
FDA Approves Astellas' Gastric Cancer Therapy
Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Brand Name : Vyloy
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 21, 2024
Details:
Astellas receives an exclusive option to license AVB-101, an investigational, AAV-based gene therapy in Phase 1/2 development for patients with frontotemporal dementia with progranulin mutations.
Lead Product(s): AVB-101
Therapeutic Area: Neurology Brand Name: AVB-101
Study Phase: Phase I/ Phase IIProduct Type: Cell and Gene therapy
Recipient: AviadoBio
Deal Size: $2,230.0 million Upfront Cash: $50 million
Deal Type: Agreement October 08, 2024
Lead Product(s) : AVB-101
Therapeutic Area : Neurology
Highest Development Status : Phase I/ Phase II
Recipient : AviadoBio
Deal Size : $2,230.0 million
Deal Type : Agreement
Astellas & AviadoBio Announce License Agreement of AVB-101 for Frontotemporal Dementia
Details : Astellas receives an exclusive option to license AVB-101, an investigational, AAV-based gene therapy in Phase 1/2 development for patients with frontotemporal dementia with progranulin mutations.
Brand Name : AVB-101
Molecule Type : Cell and Gene therapy
Upfront Cash : $50 million
October 08, 2024
Details:
Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.
Lead Product(s): Enfortumab Vedotin,Pembrolizumab
Therapeutic Area: Oncology Brand Name: Padcev
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Pfizer Inc
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 24, 2024
Lead Product(s) : Enfortumab Vedotin,Pembrolizumab
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Pfizer Inc
Deal Size : Not Applicable
Deal Type : Not Applicable
Japan Approves PADCEV™ with KEYTRUDA® for Unresectable Urothelial Carcinoma
Details : Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.
Brand Name : Padcev
Molecule Type : Large molecule
Upfront Cash : Not Applicable
September 24, 2024
Details:
Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area: Oncology Brand Name: Vyloy
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 20, 2024
Lead Product(s) : Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area : Oncology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Astellas Gets EU Approval for VYLOY with Chemotherapy in Advanced Gastric Cancer
Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Brand Name : Vyloy
Molecule Type : Large molecule
Upfront Cash : Not Applicable
September 20, 2024
Details:
Veozah (fezolinetant) is a neurokinin 3 (NK3) receptor antagonist being investigated for the treatment of vasomotor symptoms in patients with breast cancer.
Lead Product(s): Fezolinetant
Therapeutic Area: Obstetrics/Gynecology (Women’s Health) Brand Name: Veozah
Study Phase: Phase IIIProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable August 27, 2024
Lead Product(s) : Fezolinetant
Therapeutic Area : Obstetrics/Gynecology (Women’s Health)
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Astellas Begins Phase 3 Study of Fezolinetant for VMS in Breast Cancer Patients
Details : Veozah (fezolinetant) is a neurokinin 3 (NK3) receptor antagonist being investigated for the treatment of vasomotor symptoms in patients with breast cancer.
Brand Name : Veozah
Molecule Type : Small molecule
Upfront Cash : Not Applicable
August 27, 2024
Details:
Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda, a PD-1 inhibitoris approved for locally advanced or metastatic urothelial cancer.
Lead Product(s): Enfortumab Vedotin,Pembrolizumab,Cisplatin
Therapeutic Area: Oncology Brand Name: Padcev
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable August 27, 2024
Lead Product(s) : Enfortumab Vedotin,Pembrolizumab,Cisplatin
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
European Commission Approves PADCEV™ with KEYTRUDA® for Advanced Urothelial Cancer
Details : Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda, a PD-1 inhibitoris approved for locally advanced or metastatic urothelial cancer.
Brand Name : Padcev
Molecule Type : Large molecule
Upfront Cash : Not Applicable
August 27, 2024
Details:
Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.
Lead Product(s): Enfortumab Vedotin,Pembrolizumab
Therapeutic Area: Oncology Brand Name: Padcev
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Pfizer Inc
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable August 19, 2024
Lead Product(s) : Enfortumab Vedotin,Pembrolizumab
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Pfizer Inc
Deal Size : Not Applicable
Deal Type : Not Applicable
China's NMPA Approves PADCEV™ for Advanced Urothelial Cancer
Details : Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.
Brand Name : Padcev
Molecule Type : Large molecule
Upfront Cash : Not Applicable
August 19, 2024
Details:
Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area: Oncology Brand Name: Vyloy
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable July 26, 2024
Lead Product(s) : Zolbetuximab,Oxaliplatin,Capecitabine
Therapeutic Area : Oncology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Astellas Receives Positive CHMP Opinion for Zolbetuximab in Advanced Gastric Cancer
Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.
Brand Name : Vyloy
Molecule Type : Large molecule
Upfront Cash : Not Applicable
July 26, 2024
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ADENOSCAN
Dosage Strength : 60MG/20ML (3MG/ML) **F...
Packaging :
Approval Date : 1995-05-18
Application Number : 20059
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ADENOCARD
Dosage Strength : 3MG/ML **Federal Regis...
Packaging :
Approval Date : 1989-10-30
Application Number : 19937
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ADENOSCAN
Dosage Strength : 90MG/30ML (3MG/ML) **F...
Packaging :
Approval Date : 1995-05-18
Application Number : 20059
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Dosage Form :
Brand Name : Fosfalugel
Dosage Strength : 26 Bust Gel Os 15 Ml 1...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.025% **Federal Regis...
Packaging :
Approval Date : 1982-01-01
Application Number : 18116
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Registe...
Packaging :
Approval Date : 1982-01-01
Application Number : 18498
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Registe...
Packaging :
Approval Date : 1982-01-01
Application Number : 18116
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1%
Packaging :
Approval Date : 1988-06-13
Application Number : 19729
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : TAB
Brand Name : Forcid Solutab 875/125
Dosage Strength : 875mg
Packaging : 10X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : AMBISOME
Dosage Strength : 50MG/VIAL
Packaging : 1/10 VIALS (20 OR 30 ML VIALS)
Approval Date :
Application Number : 2241630
Regulatory Info :
Registration Country : Canada
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : ADENOCARD
Dosage Strength : 3MG/ML **Federal Registe...
Approval Date : 1989-10-30
Application Number : 19937
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : ADENOSCAN
Dosage Strength : 60MG/20ML (3MG/ML) **Fed...
Approval Date : 1995-05-18
Application Number : 20059
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : ADENOSCAN
Dosage Strength : 90MG/30ML (3MG/ML) **Fed...
Approval Date : 1995-05-18
Application Number : 20059
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : CYCLOCORT
Dosage Strength : 0.025% **Federal Registe...
Approval Date : 1982-01-01
Application Number : 18116
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Register ...
Approval Date : 1982-01-01
Application Number : 18116
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : OINTMENT; TOPICAL
Proprietary Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Register ...
Approval Date : 1982-01-01
Application Number : 18498
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : CYCLOCORT
Dosage Strength : 0.1%
Approval Date : 1988-06-13
Application Number : 19729
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : INJECTABLE, LIPOSOMAL; INJECTI...
Proprietary Name : AMBISOME
Dosage Strength : 50MG/VIAL
Approval Date : 1997-08-11
Application Number : 50740
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVITREAL
Proprietary Name : IZERVAY
Dosage Strength : EQ 2MG BASE/0.1ML (EQ 2M...
Approval Date : 2023-08-04
Application Number : 217225
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : CEFIZOX
Dosage Strength : EQ 500MG BASE/VIAL
Approval Date : 1983-09-15
Application Number : 50560
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Regulatory Info :
Registration Country : Italy
Dosage Form :
Dosage Strength : 26 Bust Gel Os 15 Ml 12.38 ...
Packaging :
Brand Name : Fosfalugel
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Auranofina 3Mg 30 Joined' Oral...
Dosage Strength : 30 cpr riv 3 mg
Packaging :
Brand Name : Ridaura
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Barnidipina 10Mg 28 Combined O...
Dosage Strength : 28 cps 10 mg modified relea...
Packaging :
Brand Name : Ipine
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Barnidipina 20Mg 28 Combined O...
Dosage Strength : 28 cps 20 mg modified relea...
Packaging :
Brand Name : Ipine
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Bendamustina 100Mg 5 Units Par...
Dosage Strength : 5 VIALS EV 100 mg 2,5 mg/ml
Packaging :
Brand Name : Levact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Bendamustina 25Mg 20 Joined Th...
Dosage Strength : 20 VIALS EV 25 mg 2.5 mg/ml
Packaging :
Brand Name : Levact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Bendamustina 25Mg 5 Units Pare...
Dosage Strength : 5 VIALS EV 25 mg 2.5 mg/ml
Packaging :
Brand Name : Levact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Dosage Form : Powder to concentrate to the i...
Dosage Strength : 2.5 mg/ml
Packaging : Hood glass
Brand Name : Levact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Powder to concentrate to the i...
Dosage Strength : 2.5 mg/ml
Packaging : Hood glass
Brand Name : Levact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Sweden
Dosage Form : PULVER TILL KONCENTRAT TILL
Dosage Strength : 2,5 MG/ML
Packaging :
Brand Name : Ribovact
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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ABOUT THIS PAGE
Astellas Pharma is a supplier offers 40 products (APIs, Excipients or Intermediates).
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