Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1USV Private Limited
03 1Farmhispania S. A.
04 1Exemed Pharmaceuticals
05 2Harman Finochem Ltd.
06 1Laurus Labs Limited
07 1Ningxia Hengkang Technology Co. , Ltd.
08 1SHOUGUANG FUKANG PHARMACEUTICAL CO. , LTD.
09 1Shandong Keyuan Pharmaceutical Co. , Ltd.
10 1Uquifa Mexico, S. A. de C. V.
11 1Vistin Pharma AS
12 1Wanbury Limited
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registration Number : 305MF10066
Registrant's Address : 2nd Floor, 3rd Block My Home Hub, Madhapur, Hyderabad, Telangana 500081 India
Initial Date of Registration : 2023-05-24
Latest Date of Registration : 2023-05-24
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Japanese Pharmacopoeia Metformin Hydrochloride
Registration Number : 219MF10176
Registrant's Address : Arvind Vithal Gandhi Chowk,B. S. D. Marg, Govandi, Mumbai-400 088, India
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2014-11-17
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Registration Number : 220MF10154
Registrant's Address : Balmes 85, Atico, 08008 (Barcelona), Spain
Initial Date of Registration : 2008-06-30
Latest Date of Registration : 2008-06-30
A Glucophage manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucophage, including repackagers and relabelers. The FDA regulates Glucophage manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucophage 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 Glucophage manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucophage supplier is an individual or a company that provides Glucophage active pharmaceutical ingredient (API) or Glucophage finished formulations upon request. The Glucophage suppliers may include Glucophage API manufacturers, exporters, distributors and traders.
click here to find a list of Glucophage 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 Glucophage Drug Master File in Japan (Glucophage JDMF) empowers Glucophage 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 Glucophage JDMF during the approval evaluation for pharmaceutical products. At the time of Glucophage 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 Glucophage suppliers with JDMF on PharmaCompass.
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