01 1SIGMA TAU
01 1QUINACRINE HCL.
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3905
Submission : 1980-08-08
Status : Inactive
Type : II
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A QUINACRINE HCL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QUINACRINE HCL, including repackagers and relabelers. The FDA regulates QUINACRINE HCL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QUINACRINE HCL 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 QUINACRINE HCL supplier is an individual or a company that provides QUINACRINE HCL active pharmaceutical ingredient (API) or QUINACRINE HCL finished formulations upon request. The QUINACRINE HCL suppliers may include QUINACRINE HCL API manufacturers, exporters, distributors and traders.
click here to find a list of QUINACRINE HCL suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A QUINACRINE HCL DMF (Drug Master File) is a document detailing the whole manufacturing process of QUINACRINE HCL active pharmaceutical ingredient (API) in detail. Different forms of QUINACRINE HCL DMFs exist exist since differing nations have different regulations, such as QUINACRINE HCL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A QUINACRINE HCL DMF submitted to regulatory agencies in the US is known as a USDMF. QUINACRINE HCL USDMF includes data on QUINACRINE HCL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The QUINACRINE HCL USDMF is kept confidential to protect the manufacturer’s intellectual property.
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