01 1Henkel AG & Co. KGaA
01 1FATTY ACIDS
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1011
Submission : 1966-11-21
Status : Inactive
Type : II
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A E236 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E236, including repackagers and relabelers. The FDA regulates E236 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E236 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 E236 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A E236 supplier is an individual or a company that provides E236 active pharmaceutical ingredient (API) or E236 finished formulations upon request. The E236 suppliers may include E236 API manufacturers, exporters, distributors and traders.
click here to find a list of E236 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A E236 DMF (Drug Master File) is a document detailing the whole manufacturing process of E236 active pharmaceutical ingredient (API) in detail. Different forms of E236 DMFs exist exist since differing nations have different regulations, such as E236 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A E236 DMF submitted to regulatory agencies in the US is known as a USDMF. E236 USDMF includes data on E236's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The E236 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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