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01 1SODIUM N-LAUROYL SARCOSINATE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 128
Submission : 1954-02-23
Status : Inactive
Type : II
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A N-Lauroylsarcosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Lauroylsarcosine, including repackagers and relabelers. The FDA regulates N-Lauroylsarcosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Lauroylsarcosine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A N-Lauroylsarcosine supplier is an individual or a company that provides N-Lauroylsarcosine active pharmaceutical ingredient (API) or N-Lauroylsarcosine finished formulations upon request. The N-Lauroylsarcosine suppliers may include N-Lauroylsarcosine API manufacturers, exporters, distributors and traders.
click here to find a list of N-Lauroylsarcosine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N-Lauroylsarcosine DMF (Drug Master File) is a document detailing the whole manufacturing process of N-Lauroylsarcosine active pharmaceutical ingredient (API) in detail. Different forms of N-Lauroylsarcosine DMFs exist exist since differing nations have different regulations, such as N-Lauroylsarcosine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A N-Lauroylsarcosine DMF submitted to regulatory agencies in the US is known as a USDMF. N-Lauroylsarcosine USDMF includes data on N-Lauroylsarcosine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The N-Lauroylsarcosine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of N-Lauroylsarcosine suppliers with USDMF on PharmaCompass.
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