Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a. s.
02 1SANOFI WINTHROP INDUSTRIE
03 1Teva API India Private Limited
04 2Active Pharma Inc.
05 1Assia Chemical Industries Ltd.
06 1CENTAUR PHARMACEUTICALS PRIVATE LTD.
07 1Glenmark Life Sciences Limited
08 1LUPIN LIMITED.
09 2Permakem Asia Co., Ltd.
10 1Sanyo Chemical Research Institute Co., Ltd.
11 1Tianish Laboratories Private Limited
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 218MF10589
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 779 00 Olomouc Czech Republic
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2024-02-07
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 219MF10328
Registrant's Address : 82 Avenue Raspail 94250 Gentilly (FRANCE)
Initial Date of Registration : 2007-11-05
Latest Date of Registration : 2013-12-03
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 306MF10046
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2024-03-21
Latest Date of Registration : 2024-03-21
A Zolpidem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolpidem, including repackagers and relabelers. The FDA regulates Zolpidem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolpidem 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 Zolpidem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolpidem supplier is an individual or a company that provides Zolpidem active pharmaceutical ingredient (API) or Zolpidem finished formulations upon request. The Zolpidem suppliers may include Zolpidem API manufacturers, exporters, distributors and traders.
click here to find a list of Zolpidem 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 Zolpidem Drug Master File in Japan (Zolpidem JDMF) empowers Zolpidem 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 Zolpidem JDMF during the approval evaluation for pharmaceutical products. At the time of Zolpidem 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 Zolpidem suppliers with JDMF on PharmaCompass.
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