01 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
01 1Disulfiram
01 1India
01 1Valid
Certificate Number : CEP 2019-197 - Rev 01
Status : Valid
Issue Date : 2024-07-15
Type : Chemical
Substance Number : 603
97
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 Antabus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Antabus, including repackagers and relabelers. The FDA regulates Antabus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Antabus 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 Antabus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Antabus supplier is an individual or a company that provides Antabus active pharmaceutical ingredient (API) or Antabus finished formulations upon request. The Antabus suppliers may include Antabus API manufacturers, exporters, distributors and traders.
click here to find a list of Antabus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Antabus CEP of the European Pharmacopoeia monograph is often referred to as a Antabus Certificate of Suitability (COS). The purpose of a Antabus CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Antabus EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Antabus to their clients by showing that a Antabus CEP has been issued for it. The manufacturer submits a Antabus CEP (COS) as part of the market authorization procedure, and it takes on the role of a Antabus CEP holder for the record. Additionally, the data presented in the Antabus CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Antabus DMF.
A Antabus CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Antabus 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 Antabus suppliers with CEP (COS) on PharmaCompass.
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