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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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PharmaCompass offers a list of Lauramine Oxide 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 Lauramine Oxide manufacturer or Lauramine Oxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lauramine Oxide manufacturer or Lauramine Oxide supplier.
PharmaCompass also assists you with knowing the Lauramine Oxide API Price utilized in the formulation of products. Lauramine Oxide API Price is not always fixed or binding as the Lauramine Oxide Price is obtained through a variety of data sources. The Lauramine Oxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxamin LO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxamin LO, including repackagers and relabelers. The FDA regulates Oxamin LO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxamin LO 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 Oxamin LO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxamin LO supplier is an individual or a company that provides Oxamin LO active pharmaceutical ingredient (API) or Oxamin LO finished formulations upon request. The Oxamin LO suppliers may include Oxamin LO API manufacturers, exporters, distributors and traders.
click here to find a list of Oxamin LO suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxamin LO DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxamin LO active pharmaceutical ingredient (API) in detail. Different forms of Oxamin LO DMFs exist exist since differing nations have different regulations, such as Oxamin LO USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxamin LO DMF submitted to regulatory agencies in the US is known as a USDMF. Oxamin LO USDMF includes data on Oxamin LO's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxamin LO USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxamin LO suppliers with USDMF on PharmaCompass.