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01 1DIPIVEFRINE HCL.
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5726
Submission : 1985-02-04
Status : Inactive
Type : II
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A Dipivefrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dipivefrin, including repackagers and relabelers. The FDA regulates Dipivefrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dipivefrin 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 Dipivefrin supplier is an individual or a company that provides Dipivefrin active pharmaceutical ingredient (API) or Dipivefrin finished formulations upon request. The Dipivefrin suppliers may include Dipivefrin API manufacturers, exporters, distributors and traders.
click here to find a list of Dipivefrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dipivefrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Dipivefrin active pharmaceutical ingredient (API) in detail. Different forms of Dipivefrin DMFs exist exist since differing nations have different regulations, such as Dipivefrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dipivefrin DMF submitted to regulatory agencies in the US is known as a USDMF. Dipivefrin USDMF includes data on Dipivefrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dipivefrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dipivefrin suppliers with USDMF on PharmaCompass.
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