Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI CHIMIE Gentilly FR
02 1Moehs Iberica S.L. Rubi ES
03 1HIKAL LIMITED Bangalore IN
01 3Acebutolol hydrochloride
01 1France
02 1India
03 1Spain
01 1Valid
02 2Withdrawn by Holder
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R1-CEP 1998-136 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2016-07-08
Type : Chemical
Substance Number : 871
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 1997-012 - Rev 11
Status : Valid
Issue Date : 2024-01-31
Type : Chemical
Substance Number : 871
Certificate Number : R1-CEP 2004-178 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2022-09-14
Type : Chemical
Substance Number : 871
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PharmaCompass offers a list of Acebutolol Hydrochloride 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 Acebutolol Hydrochloride manufacturer or Acebutolol Hydrochloride supplier for your needs.
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A AKOS015895193 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS015895193, including repackagers and relabelers. The FDA regulates AKOS015895193 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS015895193 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A AKOS015895193 supplier is an individual or a company that provides AKOS015895193 active pharmaceutical ingredient (API) or AKOS015895193 finished formulations upon request. The AKOS015895193 suppliers may include AKOS015895193 API manufacturers, exporters, distributors and traders.
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A AKOS015895193 CEP of the European Pharmacopoeia monograph is often referred to as a AKOS015895193 Certificate of Suitability (COS). The purpose of a AKOS015895193 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AKOS015895193 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AKOS015895193 to their clients by showing that a AKOS015895193 CEP has been issued for it. The manufacturer submits a AKOS015895193 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AKOS015895193 CEP holder for the record. Additionally, the data presented in the AKOS015895193 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AKOS015895193 DMF.
A AKOS015895193 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AKOS015895193 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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