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