01 1Syensqo
01 1DISODIUM PAMOATE MONOHYDRATE (DISP)
01 1Belgium
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3842
Submission : 1980-06-11
Status : Inactive
Type : II
A UNII-ZL7OV5621O manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-ZL7OV5621O, including repackagers and relabelers. The FDA regulates UNII-ZL7OV5621O manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-ZL7OV5621O 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 UNII-ZL7OV5621O supplier is an individual or a company that provides UNII-ZL7OV5621O active pharmaceutical ingredient (API) or UNII-ZL7OV5621O finished formulations upon request. The UNII-ZL7OV5621O suppliers may include UNII-ZL7OV5621O API manufacturers, exporters, distributors and traders.
click here to find a list of UNII-ZL7OV5621O suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A UNII-ZL7OV5621O DMF (Drug Master File) is a document detailing the whole manufacturing process of UNII-ZL7OV5621O active pharmaceutical ingredient (API) in detail. Different forms of UNII-ZL7OV5621O DMFs exist exist since differing nations have different regulations, such as UNII-ZL7OV5621O USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A UNII-ZL7OV5621O DMF submitted to regulatory agencies in the US is known as a USDMF. UNII-ZL7OV5621O USDMF includes data on UNII-ZL7OV5621O's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The UNII-ZL7OV5621O USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of UNII-ZL7OV5621O suppliers with USDMF on PharmaCompass.
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