01 1Alembic Pharmaceuticals Limited
02 1Daito Co., Ltd.
03 1HANMI FINE CHEMICAL CO. , LTD.
04 1Honor Lab Limited
01 2Linagliptin
02 1Linagliptin hydrate
03 1linagliptin hydrate
01 2India
02 1Japan
03 1South Korea
Registration Number : 305MF10137
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2023-12-19
Latest Date of Registration : 2023-12-19
Registration Number : 307MF10016
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2025-01-23
Latest Date of Registration : 2025-01-23
Registration Number : 305MF10132
Registrant's Address : 57, Gyeongje-ro, Siheung-si, Gyeonggi-do, Korea
Initial Date of Registration : 2023-12-12
Latest Date of Registration : 2023-12-12
Registration Number : 305MF10029
Registrant's Address : H. No. &8-3-166/7/1, Erragadda, Hyderabad-500018, Telangana, INDIA.
Initial Date of Registration : 2023-02-15
Latest Date of Registration : 2023-02-15
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PharmaCompass offers a list of Linagliptin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Linagliptin manufacturer or Linagliptin supplier for your needs.
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PharmaCompass also assists you with knowing the Linagliptin API Price utilized in the formulation of products. Linagliptin API Price is not always fixed or binding as the Linagliptin Price is obtained through a variety of data sources. The Linagliptin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trajenta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trajenta, including repackagers and relabelers. The FDA regulates Trajenta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trajenta API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Trajenta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trajenta supplier is an individual or a company that provides Trajenta active pharmaceutical ingredient (API) or Trajenta finished formulations upon request. The Trajenta suppliers may include Trajenta API manufacturers, exporters, distributors and traders.
click here to find a list of Trajenta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Trajenta Drug Master File in Japan (Trajenta JDMF) empowers Trajenta API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Trajenta JDMF during the approval evaluation for pharmaceutical products. At the time of Trajenta JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Trajenta suppliers with JDMF on PharmaCompass.
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