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    About

    Daiichi Sankyo is a global pharmaceutical company with corporate origins in Japan. We provide innovative products and services in more than 20 countries around the world. With more than 100 years of scientific expertise, our company draws upon a rich legacy of innovation and a robust pipeline of promising new medicines to help patients. Through the outstanding knowledge and commitment of our 15,000 employees worldwide, we crea...
    Daiichi Sankyo is a global pharmaceutical company with corporate origins in Japan. We provide innovative products and services in more than 20 countries around the world. With more than 100 years of scientific expertise, our company draws upon a rich legacy of innovation and a robust pipeline of promising new medicines to help patients. Through the outstanding knowledge and commitment of our 15,000 employees worldwide, we create innovative new and generic medicines, and new methods of drug discovery and delivery. We share a passion for innovation, as well as compassion for the patients around the world who are in need of our medicines.

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    Daiichi Sankyojapan Flag
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    Japan
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    3-5-1, Nihonbashi-honcho, Chuo-ku, Tokyo 103-8426
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    +81-3-6225-1111
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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

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    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: 2508

    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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    AZ, Daiichi promote better care for Black breast cancer patients
    AZ, Daiichi promote better care for Black breast cancer patients

    15 Oct 2024

    // FIERCE PHARMA

    https://www.fiercepharma.com/marketing/az-daiichi-back-campaign-provide-black-breast-cancer-patients-specialized-care

    FIERCE PHARMA
    15 Oct 2024
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    MILOS Study Highlights Bempedoic Acid's Potential In Dyslipidemia
    MILOS Study Highlights Bempedoic Acid's Potential In Dyslipidemia

    11 Oct 2024

    // EXPRESSPHARMA

    https://www.expresspharma.in/milos-study-highlights-potential-of-bempedoic-acid-to-advance-dyslipidemia-treatment-globaldata/

    EXPRESSPHARMA
    11 Oct 2024
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    ENHERTU® Gets Priority Review For HER2-Low Breast Cancer
    ENHERTU® Gets Priority Review For HER2-Low Breast Cancer

    01 Oct 2024

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20241001863203/en

    BUSINESSWIRE
    01 Oct 2024
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    ENHERTU Granted Priority Review For HER2 Low Breast Cancer
    ENHERTU Granted Priority Review For HER2 Low Breast Cancer

    30 Sep 2024

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20240930807595/en

    BUSINESSWIRE
    30 Sep 2024
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    MILOS German Cohort Results Show Increase In LDL-C Goal With
    MILOS German Cohort Results Show Increase In LDL-C Goal With

    27 Sep 2024

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20240926678909/en

    BUSINESSWIRE
    27 Sep 2024
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    AstraZeneca's drug disappoints in breast cancer survival trial
    AstraZeneca's drug disappoints in breast cancer survival trial

    23 Sep 2024

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/astrazenecas-experimental-cancer-drug-shows-no-significant-improvement-overall-2024-09-23/

    REUTERS
    23 Sep 2024
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    ALL APIs

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

    01

    Ofloxacin

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Ofloxacin

    Japan

    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 Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 4665

    Submission : 1982-09-28

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2003-210 - Rev 03

    Issue Date : 2015-08-04

    Type : Chemical

    Substance Number : 1455

    Status : Valid

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    Place

    02

    Olmesartan Medoxomil

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Olmesartan Medoxomil

    Japan

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

    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 11432

    Submission : 1995-04-07

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2012-398 - Rev 02

    Issue Date : 2022-05-16

    Type : Chemical

    Substance Number : 2600

    Status : Valid

     JDMF EU-WC NDC KDMF arrow-down
    ✖

    Registrant Name : Daewoong Pharmaceutical Co., Ltd.

    Registration Date : 2018-10-30

    Registration Number : 43-1-ND(1)

    Manufacturer Name : Daiichi Sankyo Chemical Pharma Co., Ltd.@[Manufacturer of Intermediate 'Olmesartan'] EUROAPI Hungary Ltd.

    Manufacturer Address : 477, Takada, Odawara, Kanagawa, Japan@[Intermediate 'Olmesartan' manufacturer] Tó utca 1-5., Budapest, 1045, Hungary

     VMF Others AUDIT
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    Market
    Place

    03

    Pravastatin

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Pravastatin

    Japan

    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 Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 5968

    Submission : 1985-08-29

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2003-122 - Rev 05

    Issue Date : 2016-06-14

    Type : Chemical

    Substance Number : 2059

    Status : Valid

     JDMF EU-WC NDC KDMF arrow-down
    ✖

    Registrant Name : HKINNOEN Co., Ltd.

    Registration Date : 2005-08-31

    Registration Number : 20050831-70-B-192-07

    Manufacturer Name : Daiichi Sankyo Chemical Pharma Co., Ltd.

    Manufacturer Address : 389-4 Izumimachi Shimokawa, Aza-ohtsurugi, Iwaki, Fukushima 971-8183, Japan

     VMF Others AUDIT
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    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    04

    Deruxtecan

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Deruxtecan

    Japan

    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 : 30003

    Submission : 2015-12-09

    Status : Active

    Type : II

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

    Stock Recap
    #PipelineProspector

    Market
    Place

    05

    Deruxtecan

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Deruxtecan

    Japan

    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 : 34021

    Submission : 2019-07-31

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    06

    Etilevodopa

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Etilevodopa

    Japan

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

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    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 5044

    Submission : 1983-08-09

    Status : Inactive

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R1-CEP 1999-091 - Rev 03

    Issue Date : 2008-05-14

    Type : Chemical

    Substance Number : 38

    Status : Withdrawn by Holder

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    Market
    Place

    07

    Human Ghrelin

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Human Ghrelin

    Japan

    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 : 18461

    Submission : 2005-06-30

    Status : Active

    Type : II

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

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    #PipelineProspector

    Market
    Place

    08

    Hydromorphone Hydrochloride

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

    2024 ACI Convention
    Not Confirmed
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    Hydromorphone Hydrochloride

    Japan

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

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

    Registration Number : 227MF10256

    Registrant's Address : 3-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo

    Initial Date of Registration : 2015-10-21

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    09

    Loxoprofen Sodium

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Loxoprofen Sodium

    Japan

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

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

    Registration Number : 221MF10083

    Registrant's Address : 4-4-8 Nishi-Yahata, Hiratsuka City, Kanagawa Prefecture

    Initial Date of Registration : 2009-04-22

    Latest Date of Registration :

    EU-WC NDC KDMF arrow-down
    ✖

    Registrant Name : Dongwha Pharmaceutical Co., Ltd.

    Registration Date : 2005-08-31

    Registration Number : 20050831-8-C-74-04

    Manufacturer Name : Daiichi Sankyo Chemical Pharma Co., Ltd.

    Manufacturer Address : 477, Takada, Odawara, Kanagawa 250-0216, Japan

     VMF Others AUDIT
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    10

    Oxycodone Hydrochloride

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

    2024 ACI Convention
    Not Confirmed
    arrow

    Oxycodone Hydrochloride

    Japan

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

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

    Registration Number : 227MF10164

    Registrant's Address : 3-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo

    Initial Date of Registration : 2015-06-18

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    USDMF

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    01

    Benicar Hctr (olmesartan Medoxomil H...

    Japan
    2024 ACI Convention
    Not Confirmed
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    02

    Benicar(tm) Tablets 5 Mg, 20 Mg And ...

    Japan
    2024 ACI Convention
    Not Confirmed
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    03

    Bulk Form Of Nimustine Hcl (nidran)

    Japan
    2024 ACI Convention
    Not Confirmed
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    04

    Carperitide Drug Substance

    Japan
    2024 ACI Convention
    Not Confirmed
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    05

    Cefmetazole (free Acid)

    Japan
    2024 ACI Convention
    Not Confirmed
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    06

    Cefmetazole Sodium Injection(vials)

    Japan
    2024 ACI Convention
    Not Confirmed
    arrow

    07

    Cetraxate Hcl Capsules

    Japan
    2024 ACI Convention
    Not Confirmed
    arrow

    08

    Cetraxate Hydrochloride

    Japan
    2024 ACI Convention
    Not Confirmed
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    09

    Cs-023 Drug Substance

    Japan
    2024 ACI Convention
    Not Confirmed
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    10

    Cs-088 Drug Substance

    Japan
    2024 ACI Convention
    Not Confirmed
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    Contact Daiichi Sankyo Co Ltd and get a quotation

    Daiichi Sankyo Co Ltd is a supplier offers 76 products (APIs, Excipients or Intermediates).

    Find a price of Ofloxacin bulk with CEP offered by Daiichi Sankyo Co Ltd

    Find a price of Olmesartan Medoxomil bulk with CEP offered by Daiichi Sankyo Co Ltd

    Find a price of Pravastatin bulk with CEP offered by Daiichi Sankyo Co Ltd

    Find a price of Codeine bulk with JDMF offered by Daiichi Sankyo Co Ltd

    Find a price of Codeine Phosphate bulk with JDMF offered by Daiichi Sankyo Co Ltd

    Find a price of Deruxtecan bulk with DMF offered by Daiichi Sankyo Co Ltd

    Find a price of Etilevodopa bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Human Ghrelin bulk with DMF offered by Daiichi Sankyo Co Ltd

    Find a price of Hydromorphone Hydrochloride bulk with JDMF offered by Daiichi Sankyo Co Ltd

    Find a price of Loxoprofen Sodium bulk with JDMF offered by Daiichi Sankyo Co Ltd

    Find a price of Oxycodone Hydrochloride bulk with JDMF offered by Daiichi Sankyo Co Ltd

    Find a price of MUCOPOLYSACCHARIDE POLYSULFATE DRUG SUBSTANCE bulk with DMF offered by Daiichi Sankyo Co Ltd

    Find a price of 2-Naphthalenepropanoic Acid bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Benfluorexum bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Carperitide bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Cefmetazole bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Cefmetazole Sodium bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Cefpodoxime Proxetil bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Cetraxate bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Cs 023 bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Edoxaban Tosylate bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Enkephalin, Methionine bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Faropenem Medoxomil bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Hydrochlorothiazide bulk offered by Daiichi Sankyo Co Ltd

    Find a price of L-VALINE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Levofloxacin bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Levofloxacin Hydrochloride bulk offered by Daiichi Sankyo Co Ltd

    Find a price of MALOTILATE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Managlinat Dialanetil bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Mepirizole bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Nimustine bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Ofloxacin bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Olmesartan Medoxomil bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Pantethine bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Phenylalanine bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Pravastatin bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Temocapril Hydrochloride bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Tranexamic Acid bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Troglitazone bulk offered by Daiichi Sankyo Co Ltd

    Find a price of Tryptophan bulk offered by Daiichi Sankyo Co Ltd

    Find a price of MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES IN SHIZUOKA JAPAN. bulk offered by Daiichi Sankyo Co Ltd

    Find a price of POLYSULFATED GLYCOSAMINOGLYCAN (PSGAG) bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DATICHI PHARMACEUTICAL CO LTD DU-6859A bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DZ-697B DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-505 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DK-507K DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-011 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of SUN N 8075 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-834 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES IN EDOGAWA-KU, TOKYO, JAPAN. bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DS-4152 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of MIX-RR bulk offered by Daiichi Sankyo Co Ltd

    Find a price of BULK CS-045 ORAL HYPOGLYCEMIC bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DS-1594B DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of SUN13837 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-505 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DW-908E DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DE-310 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-780 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-003 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-758 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-834 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of FACILITIES AND OPERATING PROCEDURES IN HIRATSUKA-SHI, JAPAN bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DF-4639 INTERMEDIATE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DL 8280 MEFOXACIN ACTIVE & PLACEBO TABS bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DS-1594B DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of SUN13834 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DX-8951F DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DX-619 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of SUN N4057 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-003 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of CS-758 DRUG PRODUCT bulk offered by Daiichi Sankyo Co Ltd

    Find a price of PANTOSIN 200 MG TABLETS bulk offered by Daiichi Sankyo Co Ltd

    Find a price of PARENTERAL FORMULATION FACILITY IN OSAKA, JAPAN. bulk offered by Daiichi Sankyo Co Ltd

    Find a price of PRODUCTION TECHNOLOGY RESEARCH LABS., EDOGAWA-KU, TOKYO, JAPAN bulk offered by Daiichi Sankyo Co Ltd

    Find a price of DT-5621 DRUG SUBSTANCE bulk offered by Daiichi Sankyo Co Ltd

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