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    About

    Our goal is to lead the way to a healthier future. But we also care about how we get there together. As a company whose products touch the lives and well being of people around the world, we hold ourselves to a high standard. And we expect others to hold us to that same high standard. We believe in operating openly, honestly and with the highest degree of ethics and integrity. This includes: making sure that the compa...
    Our goal is to lead the way to a healthier future. But we also care about how we get there together. As a company whose products touch the lives and well being of people around the world, we hold ourselves to a high standard. And we expect others to hold us to that same high standard. We believe in operating openly, honestly and with the highest degree of ethics and integrity. This includes: making sure that the company complies with all applicable laws and regulations globally.

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    Merck & CoUnited_States_of_America Flag
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    One Merck Drive, P.O. Box 100 Whitehouse Station, NJ 08889-0100
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    INTERVIEW #SpeakPharma

    [Sponsored by another company]
    “Due to its 20-year mastery in micronization, Inke has emerged a cornerstone in treating global respiratory diseases”

    “Due to its 20-year mastery in micronization, Inke has emerged a cornerstone in treating global respiratory diseases”

    This week, SpeakPharma interviews Miquel Bachs, CEO of Inke, a company with over two decades of expertise in micronization and particle engineering, and a leader in providing high-quality, effective solutions in the global fight against chronic respiratory diseases such as COPD and asthma. In this insightful conversation, Bachs shares Inke’s strategic vision, technological innovations, and commitment to sustainability, offering a comprehensive look at how the company is shaping the future of respiratory health. HIGHLIGHTS// Inke’s strategic vision/ technological innovations/ commitment to sustainability Studies suggest that 13 percent of people over 40 years of age, the world over, have chronic obstructive pulmonary disease (COPD). Given the increasing prevalence of respiratory diseases, how does Inke position itself as a leader in the development and manufacturing of respiratory APIs? Inke has established itself as a global leader in generic respiratory API development through our unique blend  of technological innovation, expertise in micronization, and a comprehensive portfolio of inhalation therapies. With over 20 years of experience in micronization and particle engineering, our ability to customize APIs to meet specific client requirements has resulted in highly effective, high-quality products tailored for respiratory therapies. The increasing prevalence of chronic respiratory diseases, such as COPD and asthma, has only underscored Inke’s pivotal role in supporting the pharmaceutical industry’s need for advanced treatments. We specialize in bronchodilators and other critical respiratory APIs that improve patient outcomes and meet the stringent regulatory requirements of global health authorities. Our end-to-end approach, from early-stage API development to commercial-scale production, ensures that we maintain the highest standards of quality, safety, and efficacy. As the market for respiratory APIs continues to evolve, Inke remains committed to expanding its portfolio to address unmet therapeutic needs. Beyond respiratory APIs, we are also prioritizing growth in CNS treatments and building on our expertise in complex molecule synthesis. This strategic focus allows us to provide an integrated solution that not only meets current market demands but also anticipates future pharmaceutical trends. HIGHLIGHTS// comprehensive portfolio of inhalation therapies/ over 20 years of experience in micronization and particle engineering/ specialize in bronchodilators and other critical respiratory APIs/ prioritizing growth in CNS treatments In the field of micronization, what differentiates Inke’s approach from that of other manufacturers of respiratory APIs? What sets Inke apart in micronization is our advanced particle size reduction technology and our dedication to precision. Our facility is equipped with various milling techniques such as Cone, Jet, and Pin mills, allowing us to reduce particle size while stabilizing the amorphous content to ensure consistent quality. Our in-depth understanding of respiratory APIs, combined with our ability to tailor solutions for each customer, results in APIs with improved solubility, stability, and bioavailability, which are critical for the efficacy of inhalation products. This, along with our exceptional quality standards and a flawless audit track record, has positioned us as a key partner for major players in the inhalation market. HIGHLIGHTS// advanced particle size reduction technology/ technological innovations/ tailor solutions/ improved solubility, stability, and bioavailability Developing complex APIs can be challenging. How does Inke ensure a smooth and successful partnership throughout the development and manufacturing process, including customization, ensuring regulatory compliance and timely delivery? At Inke, we are dedicated to fostering strong partnerships with our clients through a collaborative approach that prioritizes open communication and mutual understanding. Our commitment to quality and personalized service sets us apart in the pharmaceutical landscape. Our team takes the time to engage in comprehensive discussions to customize our solutions, ensuring alignment with client specifications across all batches and grades. This commitment to flexibility allows us to respond effectively to evolving requirements, solidifying Inke’s reputation as a reliable partner. We understand that navigating regulatory landscapes can be challenging. That's why our team is equipped to manage all aspects of the regulatory process with meticulous attention to detail. From the submission of Drug Master Files (DMFs) and Certificates of Suitability to crafting precise responses to potential Deficiency Letters, we ensure compliance at every step. Moreover, we offer extensive support in patent and intellectual property matters, providing technical assistance and guidance tailored to the specific requirements of each region. Our unwavering dedication to quality, coupled with our agile response capabilities, enables us to deliver exceptional results while maintaining transparency and trust. At Inke, we are committed to building lasting relationships that drive success for both our clients and our organization. HIGHLIGHTS// ensuring alignment with client specifications/ manage all aspects of the regulatory process/ support in patent and intellectual property matters Given Inke’s global presence, what are the key markets for growth and how does Inke plan to expand its market reach and strengthen its position in these regions? Inke is strategically focused on expanding its footprint in the European and US markets, where we continue to prioritize our efforts. The US market remains pivotal for us, especially considering our successful FDA inspections and ongoing regulatory compliance efforts that solidify our reputation. Japan is another significant market where we have established a robust presence, reflecting our commitment to high-quality manufacturing and innovation. Looking ahead, China represents a key growth opportunity for Inke. With 12 active DMFs registered, we are well-positioned to tap into this burgeoning market. Our strategy involves leveraging our existing capabilities to navigate regulatory landscapes and fostering strong partnerships within the region, thereby enhancing our market reach and influence in the pharmaceutical sector. HIGHLIGHTS// expanding footprint in the European and US markets/ China represents a key growth opportunity for Inke With Inke expanding into contract manufacturing organization (CMO) services, how does this new offering align with Inke’s broader strategic goals, and what advantages does it provide to pharmaceutical partners? At Inke, the introduction of CMO services is a natural extension of our core expertise in the development and manufacturing of high-quality generic APIs. Our expansion into CMO is part of a strategic move to diversify our service portfolio, allowing us to offer end-to-end solutions for our clients. The CMO service integrates seamlessly with our expertise in API manufacturing, particularly in micronization, which has been a key differentiator for Inke for over two decades. With our advanced particle engineering capabilities, we can offer tailored solutions that meet specific technical and regulatory requirements. Whether it is small-batch production or scaling up to commercial quantities, we offer the flexibility to accommodate a wide range of customer needs. This adaptability, paired with our deep expertise in micronization, allows us to support evolving project needs, maintaining the highest standards of consistency, quality, and performance that define Inke’s footprint. HIGHLIGHTS// CMO is part of a strategic move to diversify our service portfolio/ deep expertise in micronization What is Inke’s commitment to sustainability and corporate social responsibility and how is it integrating sustainable practices into its operations and product development? At Inke, we recognize that integrating environmental, social, and governance (ESG) principles into our operations is not just a responsibility but a pathway to long-term success. Our ESG vision is centered around aligning business growth with sustainable practices that positively impact our communities and the environment. We are dedicated to environmental responsibility, actively implementing initiatives such as efficient wastewater treatment and water reuse systems to minimize our ecological footprint. Our recent investments in energy efficiency include the installation of a 135 kWp solar panel system, which underscores our commitment to reducing emissions and resource consumption across our manufacturing and research facilities. Inke is also committed to fostering a diverse and inclusive workforce. With a notable increase in our team members, particularly in operations and quality assurance, we prioritize career development and the well-being of our employees. By adhering to high regulatory standards, we ensure our products meet stringent global requirements, enhancing our transparency and compliance. Through these initiatives, Inke aims to cultivate sustainable practices that not only support our business objectives but also contribute positively to the pharmaceutical industry and society at large. HIGHLIGHTS// integrating ESG principles/ efficient wastewater treatment and water reuse systems/ installation of a 135 kWp solar panel system/ diverse and inclusive workforce

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    https://www.pharmacompass.com/speak-pharma/due-to-its-20-year-mastery-in-micronization-inke-has-emerged-a-cornerstone-in-treating-global-respiratory-diseases

    #SpeakPharma With Inke
    28 Oct 2024
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    VLOG #PharmaReel

    [Sponsored by another company]

    DATA COMPILATION #PharmaFlow

    [Sponsored by another company]
    DMF filings hit all-time high in Q3 2024; China tops list with 58% increase in Type II submissions

    DMF filings hit all-time high in Q3 2024; China tops list with 58% increase in Type II submissions

    Drug Master Files, or DMFs, are confidential documents that play a crucial role in the pharmaceutical industry. These files, submitted to the US Food and Drug Administration (FDA), contain detailed information about ingredients, manufacturing processes, and packaging of medicines. They help the FDA oversee drug quality. Of the four types, Type II DMFs involve active pharmaceutical ingredients (APIs) for both branded and generic drugs. The third quarter (Q3) of 2024 saw Type II DMF submissions set a new record. A total of 309 Type II DMFs were submitted to the FDA during this period, a substantial 24.6 percent increase over Q3 2023 (with 248 submissions). The second quarter of 2024 too saw a remarkable increase, with 237 Type II DMFs being submitted compared to 178 in Q2 2023. View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available) China witnesses steep rise in DMF submissions, beats India with maximum filings In Q3 2024, China filed 153 DMFs submissions, marking a substantial 57.7 percent increase from the 97 submissions filed in Q3 2023. India maintained its strong position but fell to the number two spot with 110 DMFs, representing a modest 3.8 percent increase from 106 in Q3 2023. The US, which came a distant third, saw a slight decline in DMF submissions, with 13 filed in Q3 2024, as compared to 18 in Q3 2023. For several years, India had a lead in Type II DMFs. Since 2020, which marked the start of the pandemic, we have noticed a gradual increase in DMFs filed by China. This year, China has surpassed India considerably in the first three quarters. During the first nine months of 2024, China submitted 372, while India filed 286 DMFs. If this lead is maintained in Q4, DMFs from China will surpass that of India in 2024.  Amongst European countries, Spain led with seven DMFs, followed by Italy at four, and Germany and the Netherlands at three each. Among other nations, Japan contributed six while Israel submitted four DMFs. In company-wise tally, China’s Jiangsu East-Mab Biomedical Technology topped the list with an impressive 14 DMFs. On its heels were Indian companies — MSN at 13 DMFs, and Vamsi Labs and Hetero Drugs at nine DMFs each. China’s Porton Pharma and Wuxi AppTec filed five, while Shanghai Keze Yongxin Biotechnology, and Qingdao Glycogene Pharmaceutical contributed four submissions each. India's Maithri Drugs also submitted four. Japanese company Santeja filed five. Overall, Asia accounted for nearly 90 percent, with China contributing a dominant 49.5 percent of all DMF submissions. India was at 35.6 percent, the US at 4.2 percent, while Europe contributed 6.5 percent.  View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available) Diabetes, obesity, cancer, women’s health drugs emerge as hot molecules in Q3 2024 In terms of molecules, semaglutide (used for the treatment of type 2 diabetes and weight management) and relugolix (to treat prostate cancer and uterine fibroids) saw six DMF filings each in Q3 2024, indicating significant industry interest in these compounds. Following closely behind were semaglutide’s competitor tirzepatide and overactive bladder therapy vibegron, garnering four DMFs each. Finerenone (a non-steroidal drug for chronic kidney disease associated with type 2 diabetes) and voclosporin (an immunosuppressant for lupus nephritis) saw three DMFs each.  The last quarter also witnessed the introduction of 14 molecules with first-time DMFs. Among them were acetoxy empagliflozin, cabozantinib fumarate, tivozanib hydrochloride monohydrate, diosmetin, trilaciclib, clenbuterol hydrochloride, fenoterol hydrobromide, tapinarof and fezolinetant. Fezolinetant, with a DMF from Spain’s Moehs Iberica, is the active ingredient in Astellas’ Veozah, which is the first non-hormonal treatment for menopausal symptoms approved by the FDA. Tapinarof, filed by India’s Maithri Drugs, is used in Vtama, a novel steroid-free psoriasis cream. Other compounds that made their DMF debut include berotralstat, calcium phosphoryl choline chloride, phloroglucinol dihydrate, belumosudil mesylate and trimethylphloroglucinol. During Q2 2024, there were 19 drugs that saw DMF submissions for the first time, including molecules like triptorelin, sorafenib, pralsetinib, trilaciclib dihydrochloride, resmetirom (hepatology) and teneligliptin hydrochloride hydrate (metabolic disorders).  View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available)    GDUFA fee for FY 2025: The FDA’s Generic Drug User Fee Amendments (GDUFA) is a law designed to speed access to safe and effective generic drugs to the public and reduce costs to the industry. The fiscal year 2025 fee rates were published on July 31, 2024. The FDA has revised fees under GDUFA III for all categories. While there is a slight increase in the DMF fee from US$ 94,682 in 2024 to US$ 95,084 in 2025, the ANDA fee has witnessed a significant jump — from US$ 252,453 in 2024 to US$ 321,920 in 2025. FY 2024 and FY 2025 User Fee Rates Generic drug fee category Fees rates for FY 2024 Fees rates for FY 2025 Applications: Abbreviated New Drug Application (ANDA) US$ 2,52,453   US$ 3,21,920   Drug Master File (DMF) US$ 94,682 US$ 95,084 Facilities: Active Pharmaceutical Ingredient (API)—Domestic US$ 40,464 US$ 41,580 API—Foreign US$ 55,464 US$ 56,580 Finished Dosage Form (FDF)—Domestic US$ 2,20,427   US$ 2,31,952 FDF—Foreign US$ 2,35,427   US$ 2,46,952 Contract Manufacturing Organization (CMO)—Domestic US$ 52,902 US$ 55,668 CMO—Foreign US$ 67,902 US$ 70,668 GDUFA Program: Large size operation generic drug applicant US$ 17,29,629   US$ 18,91,664 Medium size operation generic drug applicant US$ 6,91,852   US$ 7,56,666 Small business generic drug applicant US$ 1,72,963   US$ 1,89,166 Our view The highlight of the last few quarters has been the sharp rise in Type II DMF filings from China. The submission of a DMF is not required by law or any FDA regulation. FDA’s DMF guideline offers guidance on acceptable approaches to meeting regulatory requirements. Moreover, DMFs establish trust in APIs from lesser-known companies. With a growing emphasis on compliance and quality assurance, it appears that Chinese drug companies are eager to demonstrate their commitment to high standards and build trust in the US market. And that’s good news for the pharmaceutical industry.   
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    Impressions: 2489

    https://www.pharmacompass.com/radio-compass-blog/dmf-filings-hit-all-time-high-in-q3-2024-china-tops-list-with-58-increase-in-type-ii-submissions

    #PharmaFlow by PHARMACOMPASS
    24 Oct 2024
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    NEWS #PharmaBuzz

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    Merck, Moderna Launch Phase 3 Trial for NSCLC Treatment
    Merck, Moderna Launch Phase 3 Trial for NSCLC Treatment

    28 Oct 2024

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20241028767283/en

    BUSINESSWIRE
    28 Oct 2024
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    Sanofi isn't sweating a potential RSV showdown with Merck
    Sanofi isn't sweating a potential RSV showdown with Merck

    26 Oct 2024

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/sanofi-shrugs-potential-infant-rsv-competition-merck-beyfortus-grows-sales-382

    FIERCE PHARMA
    26 Oct 2024
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    Merck buys cancer therapy developer Modifi for up to $1.3 bln
    Merck buys cancer therapy developer Modifi for up to $1.3 bln

    24 Oct 2024

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/merck-buys-cancer-therapy-developer-modifi-biosciences-up-13-bln-2024-10-23/

    REUTERS
    24 Oct 2024
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    In boon for Pfizer and Merck, CDC panel backs expanded use of vaccines
    In boon for Pfizer and Merck, CDC panel backs expanded use of vaccines

    24 Oct 2024

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/cdc-immunization-committee-votes-widen-recommendation-pneumococcal-vaccines-pfizer-merck

    FIERCE PHARMA
    24 Oct 2024
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    Merck’s KEYTRUDA® Receives New Approvals For Gynecologic Cancers
    Merck’s KEYTRUDA® Receives New Approvals For Gynecologic Cancers

    24 Oct 2024

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20241024667359/en

    BUSINESSWIRE
    24 Oct 2024
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    Merck-Gilead long-acting oral combo suppresses HIV for 48 weeks
    Merck-Gilead long-acting oral combo suppresses HIV for 48 weeks

    22 Oct 2024

    // FIERCE BIOTECH

    https://www.fiercebiotech.com/biotech/merck-gilead-long-acting-oral-combo-suppresses-hiv-48-weeks-setting-stage-pivotal-program

    FIERCE BIOTECH
    22 Oct 2024
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    ALL APIs

    read-moreClick the button for full data set
    read-moreClick the button for full data set

    01

    Betamethasone

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Betamethasone

    U.S.A

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 12937

    Submission : 1998-04-03

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2017-092 - Rev 00

    Issue Date : 2022-12-12

    Type : Chemical

    Substance Number : 312

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    02

    Betamethasone

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Betamethasone

    U.S.A

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2012-214 - Rev 00

    Issue Date : 2020-01-27

    Type : Chemical

    Substance Number : 312

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    03

    Betamethasone

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Betamethasone

    Singapore

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS JDMF arrow-down
    ✖

    Registration Number : 224MF10129

    Registrant's Address : 50 Tuas West Drive Singapore 638408

    Initial Date of Registration : 2012-07-19

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    04

    Betamethasone Dipropionate

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Betamethasone Dipropionate

    Singapore

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS JDMF arrow-down
    ✖

    Registration Number : 218MF10865

    Registrant's Address : 50 Tuas West Drive Singapore 638408

    Initial Date of Registration : 2006-11-06

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    05

    Betamethasone Valerate

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Betamethasone Valerate

    Singapore

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS JDMF arrow-down
    ✖

    Registration Number : 218MF10825

    Registrant's Address : 50 Tuas West Drive Singapore 638408

    Initial Date of Registration : 2006-10-20

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    06

    Ivermectin

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Ivermectin

    U.S.A

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2001-146 - Rev 01

    Issue Date : 2008-11-27

    Type : Chemical

    Substance Number : 1336

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Inactive-api
    ✖

    VMF Number : 5476

    Submission : 1993-10-22

    Status : Inactive

    Type : II

     Others AUDIT
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    07

    Loratadine

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Loratadine

    Singapore

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 13032

    Submission : 1998-06-18

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    08

    Loratadine

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Loratadine

    U.S.A

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth 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 CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2007-218 - Rev 00

    Issue Date : 2013-12-19

    Type : Chemical

    Substance Number : 2124

    Status : Valid

     JDMF EU-WC NDC KDMF arrow-down
    ✖

    Registrant Name : Korea MSD Co., Ltd.

    Registration Date : 2009-09-24

    Registration Number : 20090924-6-C-263-06

    Manufacturer Name : Schering-Plough (Avondale) Co

    Manufacturer Address : Rathdrum Co. Wicklow

     VMF Others AUDIT
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    09

    Montelukast Sodium

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Montelukast Sodium

    Singapore

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

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    2024 ACI Convention
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    USDMF CEP/COS JDMF arrow-down
    ✖

    Registration Number : 217MF10593

    Registrant's Address : Ballydine, Kilsheelan, Clonmel, Co. Tipperary, Ireland

    Initial Date of Registration : 2005-09-14

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    Sitagliptin Phosphate

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

    2024 ACI Convention
    Not Confirmed
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    Sitagliptin Phosphate

    Singapore

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

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    ✖

    Registration Number : 231MF10016

    Registrant's Address : 50 Tuas West Drive Singapore 638408

    Initial Date of Registration : 2019-01-23

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    01

    Brand Name : Vaxneuvance

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Vaxneuvance

    U.S.A
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    SupplySide West 2024
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    Regulatory Info :

    Registration Country : Switzerland

    15-valent Pneumococcal Polysaccharide Crm Conjugat...

    Merck & Co

    Dosage Form : Inj Susp

    Brand Name : Vaxneuvance

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    Brand Name : Vaxneuvance

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Vaxneuvance

    U.S.A
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    Registration Country : Switzerland

    15-valent Pneumococcal Polysaccharide Crm Conjugat...

    Merck & Co

    Dosage Form : Inj Susp

    Brand Name : Vaxneuvance

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    Registration Country : Switzerland

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    03

    Brand Name : Campral

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Campral

    U.S.A
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    SupplySide West 2024
    Not Confirmed
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    Regulatory Info :

    Registration Country : Switzerland

    Acamprosatum

    Merck & Co

    Dosage Form : Filmtablet

    Brand Name : Campral

    Dosage Strength : 300mg

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    Registration Country : Switzerland

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    Brand Name : Campral

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    U.S.A
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    SupplySide West 2024
    Not Confirmed
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    Regulatory Info :

    Registration Country : Switzerland

    Acamprosatum

    Merck & Co

    Dosage Form : Film-Coated Tablets

    Brand Name : Campral

    Dosage Strength : 300mg

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    Registration Country : Switzerland

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    Brand Name : DRIXORAL PLUS

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : DRIXORAL PLUS

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ACETAMINOPHEN; DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE

    Merck & Co

    Dosage Form : TABLET, EXTENDED RELEASE...

    Brand Name : DRIXORAL PLUS

    Dosage Strength : 500MG;3MG;60MG

    Packaging :

    Approval Date : 1987-05-22

    Application Number : 19453

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : Fosavance weekly tab...

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Fosavance weekly tab...

    U.S.A
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    Regulatory Info :

    Registration Country : Switzerland

    Acidum alendronicum; cholecalciferol (vitamin D3)

    Organon

    Dosage Form : Tabl

    Brand Name : Fosavance weekly tablets

    Dosage Strength : 70/2800

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    Approval Date :

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    Registration Country : Switzerland

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    07

    Brand Name : Fosavance weekly tab...

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Fosavance weekly tab...

    U.S.A
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    SupplySide West 2024
    Not Confirmed
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    Regulatory Info :

    Registration Country : Switzerland

    Acidum alendronicum; cholecalciferol (vitamin D3)

    Organon

    Dosage Form : Tabl

    Brand Name : Fosavance weekly tablets

    Dosage Strength : 70/5600

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    Approval Date :

    Application Number :

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    Registration Country : Switzerland

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    Brand Name : Fosavance weekly tab...

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Fosavance weekly tab...

    U.S.A
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    Regulatory Info :

    Registration Country : Switzerland

    Acidum alendronicum; cholecalciferol (vitamin D3)

    Organon

    Dosage Form : Tabl

    Brand Name : Fosavance weekly tablets

    Dosage Strength : 70/2800

    Packaging :

    Approval Date :

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    Regulatory Info :

    Registration Country : Switzerland

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    Brand Name : Fosavance weekly tab...

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : Fosavance weekly tab...

    U.S.A
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    SupplySide West 2024
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    Regulatory Info :

    Registration Country : Switzerland

    Acidum alendronicum; cholecalciferol (vitamin D3)

    Organon

    Dosage Form : Tabl

    Brand Name : Fosavance weekly tablets

    Dosage Strength : 70/5600

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Switzerland

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    Brand Name : FOSAMAX

    U.S.A
    SupplySide West 2024
    Not Confirmed
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    Brand Name : FOSAMAX

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ALENDRONATE SODIUM

    Organon

    Dosage Form : TABLET;ORAL

    Brand Name : FOSAMAX

    Dosage Strength : EQ 10MG BASE **Federal...

    Packaging :

    Approval Date : 1995-09-29

    Application Number : 20560

    Regulatory Info : DISCN

    Registration Country : USA

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    01

    PRODUCT 8198 TABLETING AID T

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

    SupplySide West 2024
    Not Confirmed
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    PRODUCT 8198 TABLETING AID T

    U.S.A

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

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    SupplySide West 2024
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 3796

    Submission : 1980-05-01

    Status : Inactive

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    POLYVINYL ACETATE-CROTONIC ACID COP...

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

    SupplySide West 2024
    Not Confirmed
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    POLYVINYL ACETATE-CROTONIC ACID COP...

    U.S.A

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

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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 11859

    Submission : 1996-02-16

    Status : Inactive

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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