SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 1Anjan Drug Private Limited
03 1Mitsubishi Chemical Corporation
01 1Valproic Acid
02 2Valproic acid
01 1India
02 1Japan
03 1Taiwan
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 220MF10111
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2008-04-21
Latest Date of Registration : 2008-04-21
Registration Number : 303MF10181
Registrant's Address : 5th floor, Nelson Towers II wing, 117, Nelson Manickam Road, Aminjikarai, Chennai - 6...
Initial Date of Registration : 2021-12-15
Latest Date of Registration : 2021-12-15
Registration Number : 218MF10601
Registrant's Address : 1-1-1 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
A Divalproex Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Divalproex Sodium, including repackagers and relabelers. The FDA regulates Divalproex Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Divalproex Sodium 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 Divalproex Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Divalproex Sodium supplier is an individual or a company that provides Divalproex Sodium active pharmaceutical ingredient (API) or Divalproex Sodium finished formulations upon request. The Divalproex Sodium suppliers may include Divalproex Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Divalproex Sodium 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 Divalproex Sodium Drug Master File in Japan (Divalproex Sodium JDMF) empowers Divalproex Sodium 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 Divalproex Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Divalproex Sodium 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 Divalproex Sodium suppliers with JDMF on PharmaCompass.
We have 3 companies offering Divalproex Sodium
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