01 1SAFC
01 1FENBENDAZOLE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11755
Submission : 1995-11-27
Status : Inactive
Type : II
A Oxfendazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxfendazole, including repackagers and relabelers. The FDA regulates Oxfendazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxfendazole API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Oxfendazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxfendazole supplier is an individual or a company that provides Oxfendazole active pharmaceutical ingredient (API) or Oxfendazole finished formulations upon request. The Oxfendazole suppliers may include Oxfendazole API manufacturers, exporters, distributors and traders.
click here to find a list of Oxfendazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxfendazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxfendazole active pharmaceutical ingredient (API) in detail. Different forms of Oxfendazole DMFs exist exist since differing nations have different regulations, such as Oxfendazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxfendazole DMF submitted to regulatory agencies in the US is known as a USDMF. Oxfendazole USDMF includes data on Oxfendazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxfendazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxfendazole suppliers with USDMF on PharmaCompass.
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