Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 1SANOFI-AVENTIS DEUTSCHLAND GMBH Frankfurt am Main DE
02 1FDC Limited Mumbai IN
03 1INDOCO REMEDIES LIMITED Mumbai IN
04 1OLON S.P.A. Rodano IT
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01 4Betaxolol hydrochloride
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01 1Germany
02 2India
03 1Italy
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01 3Valid
02 1Withdrawn 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 2009-344 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2016-12-08
Type : Chemical
Substance Number : 1072
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Certificate Number : CEP 2022-334 - Rev 01
Status : Valid
Issue Date : 2025-10-06
Type : Chemical
Substance Number : 1072

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Certificate Number : R1-CEP 2011-031 - Rev 01
Status : Valid
Issue Date : 2020-04-07
Type : Chemical
Substance Number : 1072

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Certificate Number : CEP 2004-154 - Rev 06
Status : Valid
Issue Date : 2024-09-03
Type : Chemical
Substance Number : 1072

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A alo 1401-02 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of alo 1401-02, including repackagers and relabelers. The FDA regulates alo 1401-02 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. alo 1401-02 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 alo 1401-02 supplier is an individual or a company that provides alo 1401-02 active pharmaceutical ingredient (API) or alo 1401-02 finished formulations upon request. The alo 1401-02 suppliers may include alo 1401-02 API manufacturers, exporters, distributors and traders.
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A alo 1401-02 CEP of the European Pharmacopoeia monograph is often referred to as a alo 1401-02 Certificate of Suitability (COS). The purpose of a alo 1401-02 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of alo 1401-02 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of alo 1401-02 to their clients by showing that a alo 1401-02 CEP has been issued for it. The manufacturer submits a alo 1401-02 CEP (COS) as part of the market authorization procedure, and it takes on the role of a alo 1401-02 CEP holder for the record. Additionally, the data presented in the alo 1401-02 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the alo 1401-02 DMF.
A alo 1401-02 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. alo 1401-02 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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