01 1BASF SE Ludwigshafen DE
02 3DSM Nutritional Products Ltd. Kaiseraugst CH
01 1RRR-alpha-Tocopheryl acetate
02 2all-rac-alpha-Tocopheryl acetate
03 1alpha-Tocopheryl acetate concentrate (powder form), 50 g per 100 g of concentrate
01 1Germany
02 3U.S.A
01 3Valid
02 1Withdrawn by Holder
All-rac-alpha-Tocopheryl Acetate
Certificate Number : R1-CEP 2005-040 - Rev 02
Status : Valid
Issue Date : 2023-06-29
Type : Chemical
Substance Number : 439
Alpha-Tocopheryl Acetate Concentrate (powder For...
Certificate Number : R0-CEP 2019-086 - Rev 00
Status : Valid
Issue Date : 2021-03-04
Type : Chemical
Substance Number : 691
All-rac-alpha-Tocopheryl Acetate
Certificate Number : R1-CEP 2001-180 - Rev 01
Status : Valid
Issue Date : 2019-05-03
Type : Chemical
Substance Number : 439
Certificate Number : R1-CEP 2001-320 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2014-10-17
Type : Chemical
Substance Number : 1257
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PharmaCompass offers a list of Vitamin E Acetate 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 Vitamin E Acetate manufacturer or Vitamin E Acetate supplier for your needs.
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A INFUVITE ADULT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INFUVITE ADULT, including repackagers and relabelers. The FDA regulates INFUVITE ADULT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INFUVITE ADULT 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 INFUVITE ADULT supplier is an individual or a company that provides INFUVITE ADULT active pharmaceutical ingredient (API) or INFUVITE ADULT finished formulations upon request. The INFUVITE ADULT suppliers may include INFUVITE ADULT API manufacturers, exporters, distributors and traders.
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A INFUVITE ADULT CEP of the European Pharmacopoeia monograph is often referred to as a INFUVITE ADULT Certificate of Suitability (COS). The purpose of a INFUVITE ADULT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of INFUVITE ADULT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of INFUVITE ADULT to their clients by showing that a INFUVITE ADULT CEP has been issued for it. The manufacturer submits a INFUVITE ADULT CEP (COS) as part of the market authorization procedure, and it takes on the role of a INFUVITE ADULT CEP holder for the record. Additionally, the data presented in the INFUVITE ADULT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the INFUVITE ADULT DMF.
A INFUVITE ADULT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. INFUVITE ADULT 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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