Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI CHIMIE Gentilly FR
02 2Moehs Iberica S.L. Rubi ES
03 1HIKAL LIMITED Bangalore IN
01 4Acebutolol hydrochloride
01 1France
02 1India
03 2Spain
01 1Valid
02 3Withdrawn 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Status : Withdrawn by Holder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Status : Withdrawn by Holder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
Certificate Number : R1-CEP 2001-389 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2016-04-21
Type : Chemical
Substance Number : 871
A Acebutolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acebutolol Hydrochloride, including repackagers and relabelers. The FDA regulates Acebutolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acebutolol Hydrochloride 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 Acebutolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acebutolol Hydrochloride supplier is an individual or a company that provides Acebutolol Hydrochloride active pharmaceutical ingredient (API) or Acebutolol Hydrochloride finished formulations upon request. The Acebutolol Hydrochloride suppliers may include Acebutolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Acebutolol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acebutolol Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Acebutolol Hydrochloride Certificate of Suitability (COS). The purpose of a Acebutolol Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acebutolol Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acebutolol Hydrochloride to their clients by showing that a Acebutolol Hydrochloride CEP has been issued for it. The manufacturer submits a Acebutolol Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acebutolol Hydrochloride CEP holder for the record. Additionally, the data presented in the Acebutolol Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acebutolol Hydrochloride DMF.
A Acebutolol Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acebutolol Hydrochloride 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 Acebutolol Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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