01 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
01 1Disulfiram
01 1India
01 1Valid
Certificate Number : CEP 2019-197 - Rev 02
Status : Valid
Issue Date : 2025-05-23
Type : Chemical
Substance Number : 603
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PharmaCompass offers a list of Sulfiram 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 Sulfiram manufacturer or Sulfiram supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfiram manufacturer or Sulfiram supplier.
PharmaCompass also assists you with knowing the Sulfiram API Price utilized in the formulation of products. Sulfiram API Price is not always fixed or binding as the Sulfiram Price is obtained through a variety of data sources. The Sulfiram Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Contralin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Contralin, including repackagers and relabelers. The FDA regulates Contralin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Contralin 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 Contralin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Contralin supplier is an individual or a company that provides Contralin active pharmaceutical ingredient (API) or Contralin finished formulations upon request. The Contralin suppliers may include Contralin API manufacturers, exporters, distributors and traders.
click here to find a list of Contralin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Contralin CEP of the European Pharmacopoeia monograph is often referred to as a Contralin Certificate of Suitability (COS). The purpose of a Contralin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Contralin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Contralin to their clients by showing that a Contralin CEP has been issued for it. The manufacturer submits a Contralin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Contralin CEP holder for the record. Additionally, the data presented in the Contralin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Contralin DMF.
A Contralin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Contralin 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 Contralin suppliers with CEP (COS) on PharmaCompass.
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