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01 1ANTINEOPLASTON A10 INJECTIONS
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10311
Submission : 1993-06-28
Status : Inactive
Type : II
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A Antineoplaston A10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Antineoplaston A10, including repackagers and relabelers. The FDA regulates Antineoplaston A10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Antineoplaston A10 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 Antineoplaston A10 supplier is an individual or a company that provides Antineoplaston A10 active pharmaceutical ingredient (API) or Antineoplaston A10 finished formulations upon request. The Antineoplaston A10 suppliers may include Antineoplaston A10 API manufacturers, exporters, distributors and traders.
click here to find a list of Antineoplaston A10 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Antineoplaston A10 DMF (Drug Master File) is a document detailing the whole manufacturing process of Antineoplaston A10 active pharmaceutical ingredient (API) in detail. Different forms of Antineoplaston A10 DMFs exist exist since differing nations have different regulations, such as Antineoplaston A10 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Antineoplaston A10 DMF submitted to regulatory agencies in the US is known as a USDMF. Antineoplaston A10 USDMF includes data on Antineoplaston A10's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Antineoplaston A10 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Antineoplaston A10 suppliers with USDMF on PharmaCompass.
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