01 1BASF
02 1Royal DSM
01 1DL-ALPHA-TOCOPHERYL ACETATE
02 1VITAMIN E ACETATE
01 1Germany
02 1Netherlands
01 1Active
02 1Inactive
01 1Complete
02 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5818
Submission : 1985-05-06
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-07-11
Pay. Date : 2017-01-10
DMF Number : 30673
Submission : 2016-07-21
Status : Active
Type : II
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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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard 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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard suppliers may include All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
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A All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard DMF (Drug Master File) is a document detailing the whole manufacturing process of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) in detail. Different forms of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard DMFs exist exist since differing nations have different regulations, such as All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard DMF submitted to regulatory agencies in the US is known as a USDMF. All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard USDMF includes data on All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard USDMF is kept confidential to protect the manufacturer’s intellectual property.
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