01 1SIGMA TAU
01 1STEARYLAMINE AS PROCESSED BY ARMAK FOR SIGMA F & D
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5264
Submission : 1983-07-27
Status : Inactive
Type : II
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PharmaCompass offers a list of Stearylamine 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 Stearylamine manufacturer or Stearylamine supplier for your needs.
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A Armeen 18D manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Armeen 18D, including repackagers and relabelers. The FDA regulates Armeen 18D manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Armeen 18D 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 Armeen 18D supplier is an individual or a company that provides Armeen 18D active pharmaceutical ingredient (API) or Armeen 18D finished formulations upon request. The Armeen 18D suppliers may include Armeen 18D API manufacturers, exporters, distributors and traders.
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A Armeen 18D DMF (Drug Master File) is a document detailing the whole manufacturing process of Armeen 18D active pharmaceutical ingredient (API) in detail. Different forms of Armeen 18D DMFs exist exist since differing nations have different regulations, such as Armeen 18D USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Armeen 18D DMF submitted to regulatory agencies in the US is known as a USDMF. Armeen 18D USDMF includes data on Armeen 18D's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Armeen 18D USDMF is kept confidential to protect the manufacturer’s intellectual property.
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