Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi Winthrop Industrie Gentilly FR
02 1SCI PHARMTECH, INC. Taoyuan City TW
03 1ANJAN DRUG PRIVATE LIMITED Alathur IN
04 1ASSURGEN PHARMA PVT LTD Lalamkoduru Village IN
05 1DUPONT NUTRITION BIOSCIENCES APS Brabrand DK
06 1HARMAN FINOCHEM LIMITED Mumbai IN
07 2Katwijk Chemie BV Katwijk ZH NL
08 3SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 2004-198 - Rev 05
Status : Valid
Issue Date : 2024-02-06
Type : Chemical
Substance Number : 678
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : R1-CEP 2004-302 - Rev 04
Status : Valid
Issue Date : 2019-07-26
Type : Chemical
Substance Number : 678
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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 CEP of the European Pharmacopoeia monograph is often referred to as a Orfiril Certificate of Suitability (COS). The purpose of a Orfiril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Orfiril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Orfiril to their clients by showing that a Orfiril CEP has been issued for it. The manufacturer submits a Orfiril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Orfiril CEP holder for the record. Additionally, the data presented in the Orfiril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Orfiril DMF.
A Orfiril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Orfiril CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Orfiril suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Orfiril
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