Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
02 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
03 2CIPLA LIMITED Mumbai IN
04 1FDC Limited Mumbai IN
05 1GlaxoSmithKline Research & Development Limited London GB
06 1LUSOCHIMICA S.P.A. Lomagna IT
07 2MELODY HEALTHCARE PVT. LTD. Mumbai IN
08 1OLON S.P.A. Rodano IT
09 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : CEP 2019-037 - Rev 01
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 687
51
PharmaCompass offers a list of Salbutamol Sulphate 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 Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier for your needs.
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A ALBUTEROL SULFATE [USP IMPURITY] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALBUTEROL SULFATE [USP IMPURITY], including repackagers and relabelers. The FDA regulates ALBUTEROL SULFATE [USP IMPURITY] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALBUTEROL SULFATE [USP IMPURITY] 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 ALBUTEROL SULFATE [USP IMPURITY] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALBUTEROL SULFATE [USP IMPURITY] supplier is an individual or a company that provides ALBUTEROL SULFATE [USP IMPURITY] active pharmaceutical ingredient (API) or ALBUTEROL SULFATE [USP IMPURITY] finished formulations upon request. The ALBUTEROL SULFATE [USP IMPURITY] suppliers may include ALBUTEROL SULFATE [USP IMPURITY] API manufacturers, exporters, distributors and traders.
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A ALBUTEROL SULFATE [USP IMPURITY] CEP of the European Pharmacopoeia monograph is often referred to as a ALBUTEROL SULFATE [USP IMPURITY] Certificate of Suitability (COS). The purpose of a ALBUTEROL SULFATE [USP IMPURITY] CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ALBUTEROL SULFATE [USP IMPURITY] EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ALBUTEROL SULFATE [USP IMPURITY] to their clients by showing that a ALBUTEROL SULFATE [USP IMPURITY] CEP has been issued for it. The manufacturer submits a ALBUTEROL SULFATE [USP IMPURITY] CEP (COS) as part of the market authorization procedure, and it takes on the role of a ALBUTEROL SULFATE [USP IMPURITY] CEP holder for the record. Additionally, the data presented in the ALBUTEROL SULFATE [USP IMPURITY] CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ALBUTEROL SULFATE [USP IMPURITY] DMF.
A ALBUTEROL SULFATE [USP IMPURITY] CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ALBUTEROL SULFATE [USP IMPURITY] CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 9 companies offering ALBUTEROL SULFATE [USP IMPURITY]
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