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01 1M/s Sun Pharmaceutical Industries Ltd
02 1M/s. Harman Finochem Ltd
03 2M/s. Sun Pharmaceuticals Industries Ltd.
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01 1Sodium Valproate (BP/EP)/Magnesium Valproate
02 1Sodium Valproate (EP/BP)
03 1Sodium Valproate BP/EP
04 1Sodium Valproate EP
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01 1WC-0044
02 1WC-0159
03 1WC-0243
04 1WC-243
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01 4India
Date of Issue : 2022-06-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0044
Address of the Firm : A-100, A-100/1, 2 & D-1, MIDC Ind. Area, Shendra, Aurangabad-431 210
Date of Issue : 2022-09-30
Valid Till : 2025-09-10
Written Confirmation Number : WC-0243
Address of the Firm : Sathammai Village, Karunkuzhi Post, Madhuranthagam Taluk, Kancheepuram District,...
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm : A-7/A-8, MIDC, Ahmednagar-414 111, Maharashtra State
Sodium Valproate (BP/EP)/Magnesium Valproate
Date of Issue : 2019-09-11
Valid Till : 2022-09-10
Written Confirmation Number : WC-243
Address of the Firm : Sathammai Village, Karunkuzhi Post, Madhranthagam Taluk, Kancheepuram District...
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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 Orfiril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orfiril, including repackagers and relabelers. The FDA regulates Orfiril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orfiril 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 Orfiril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Orfiril supplier is an individual or a company that provides Orfiril active pharmaceutical ingredient (API) or Orfiril finished formulations upon request. The Orfiril suppliers may include Orfiril API manufacturers, exporters, distributors and traders.
click here to find a list of Orfiril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Orfiril written confirmation (Orfiril WC) is an official document issued by a regulatory agency to a Orfiril manufacturer, verifying that the manufacturing facility of a Orfiril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Orfiril APIs or Orfiril finished pharmaceutical products to another nation, regulatory agencies frequently require a Orfiril WC (written confirmation) as part of the regulatory process.
click here to find a list of Orfiril suppliers with Written Confirmation (WC) on PharmaCompass.
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