01 1Pfizer Inc
01 1AT-125 (U-42,126) ANTI-TUMOR AGENT
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3566
Submission : 1979-07-20
Status : Inactive
Type : II
A Acivicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acivicin, including repackagers and relabelers. The FDA regulates Acivicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acivicin 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 Acivicin supplier is an individual or a company that provides Acivicin active pharmaceutical ingredient (API) or Acivicin finished formulations upon request. The Acivicin suppliers may include Acivicin API manufacturers, exporters, distributors and traders.
click here to find a list of Acivicin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acivicin DMF (Drug Master File) is a document detailing the whole manufacturing process of Acivicin active pharmaceutical ingredient (API) in detail. Different forms of Acivicin DMFs exist exist since differing nations have different regulations, such as Acivicin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Acivicin DMF submitted to regulatory agencies in the US is known as a USDMF. Acivicin USDMF includes data on Acivicin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Acivicin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Acivicin suppliers with USDMF on PharmaCompass.
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