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 2Katwijk Chemie bv
04 1Kyowa Pharma Chemical Co., Ltd.
05 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia sodium valproate
02 2Japanese Pharmacopoeia sodium valproate (production only)
03 2Sodium Valproate
04 1Sodium valproate
01 1India
02 2Japan
03 2Netherlands
04 1Taiwan
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 229MF10059
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2017-03-03
Latest Date of Registration : 2017-03-03
Registration Number : 305MF10098
Registrant's Address : GPD Admin Block, Plot No. 85-88, 105-109 & 112-116, SIPCOT Export Promotion Industria...
Initial Date of Registration : 2023-08-22
Latest Date of Registration : 2023-08-22
Registration Number : 304MF10081
Registrant's Address : Snijderstraat 6,2222 BA, Katwijk, ZH The Netherlands
Initial Date of Registration : 2022-05-25
Latest Date of Registration : 2022-05-25
Japanese Pharmacopoeia Sodium Valproate (for manufacturing only)
Registration Number : 218MF10526
Registrant's Address : Snijderstraat 6,2222 BA, Katwijk, ZH The Netherlands
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2006-05-18
Japanese Pharmacopoeia Sodium Valproate (for manufacturing only)
Registration Number : 228MF10202
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2016-10-31
Latest Date of Registration : 2016-10-31
Japanese Pharmacopoeia Sodium Valproate
Registration Number : 217MF10074
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2007-12-19
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PharmaCompass offers a list of Sodium Valproate 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 Sodium Valproate manufacturer or Sodium Valproate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Valproate manufacturer or Sodium Valproate supplier.
PharmaCompass also assists you with knowing the Sodium Valproate API Price utilized in the formulation of products. Sodium Valproate API Price is not always fixed or binding as the Sodium Valproate Price is obtained through a variety of data sources. The Sodium Valproate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Valproate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Valproate, including repackagers and relabelers. The FDA regulates Sodium Valproate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Valproate 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 Sodium Valproate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Valproate supplier is an individual or a company that provides Sodium Valproate active pharmaceutical ingredient (API) or Sodium Valproate finished formulations upon request. The Sodium Valproate suppliers may include Sodium Valproate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Valproate 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 Sodium Valproate Drug Master File in Japan (Sodium Valproate JDMF) empowers Sodium Valproate 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 Sodium Valproate JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Valproate 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 Sodium Valproate suppliers with JDMF on PharmaCompass.
We have 5 companies offering Sodium Valproate
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