01 1Pfizer Inc
01 1VIOMYCIN SULFATE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13380
Submission : 1998-09-01
Status : Inactive
Type : II
A Viomycin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viomycin Sulfate, including repackagers and relabelers. The FDA regulates Viomycin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viomycin Sulfate 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 Viomycin Sulfate supplier is an individual or a company that provides Viomycin Sulfate active pharmaceutical ingredient (API) or Viomycin Sulfate finished formulations upon request. The Viomycin Sulfate suppliers may include Viomycin Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Viomycin Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Viomycin Sulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Viomycin Sulfate active pharmaceutical ingredient (API) in detail. Different forms of Viomycin Sulfate DMFs exist exist since differing nations have different regulations, such as Viomycin Sulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Viomycin Sulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Viomycin Sulfate USDMF includes data on Viomycin Sulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Viomycin Sulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Viomycin Sulfate suppliers with USDMF on PharmaCompass.
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