01 1Merck & Co
01 1THIABENDAZOLE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 551
Submission : 1963-04-19
Status : Inactive
Type : II
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A Thiabendazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiabendazole, including repackagers and relabelers. The FDA regulates Thiabendazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiabendazole 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 Thiabendazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Thiabendazole supplier is an individual or a company that provides Thiabendazole active pharmaceutical ingredient (API) or Thiabendazole finished formulations upon request. The Thiabendazole suppliers may include Thiabendazole API manufacturers, exporters, distributors and traders.
click here to find a list of Thiabendazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Thiabendazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Thiabendazole active pharmaceutical ingredient (API) in detail. Different forms of Thiabendazole DMFs exist exist since differing nations have different regulations, such as Thiabendazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Thiabendazole DMF submitted to regulatory agencies in the US is known as a USDMF. Thiabendazole USDMF includes data on Thiabendazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Thiabendazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
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