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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2080
Submission : 1973-03-08
Status : Inactive
Type : II
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A Lauramine Oxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lauramine Oxide, including repackagers and relabelers. The FDA regulates Lauramine Oxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lauramine Oxide 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 Lauramine Oxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lauramine Oxide supplier is an individual or a company that provides Lauramine Oxide active pharmaceutical ingredient (API) or Lauramine Oxide finished formulations upon request. The Lauramine Oxide suppliers may include Lauramine Oxide API manufacturers, exporters, distributors and traders.
click here to find a list of Lauramine Oxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lauramine Oxide DMF (Drug Master File) is a document detailing the whole manufacturing process of Lauramine Oxide active pharmaceutical ingredient (API) in detail. Different forms of Lauramine Oxide DMFs exist exist since differing nations have different regulations, such as Lauramine Oxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lauramine Oxide DMF submitted to regulatory agencies in the US is known as a USDMF. Lauramine Oxide USDMF includes data on Lauramine Oxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lauramine Oxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lauramine Oxide suppliers with USDMF on PharmaCompass.
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