01 1Anmol Chemicals
01 1BUTYLATED HYDROXYTOLUENE USP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41970
Submission : 2025-08-09
Status : Active
Type : IV
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A Antox QT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Antox QT, including repackagers and relabelers. The FDA regulates Antox QT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Antox QT 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 Antox QT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Antox QT supplier is an individual or a company that provides Antox QT active pharmaceutical ingredient (API) or Antox QT finished formulations upon request. The Antox QT suppliers may include Antox QT API manufacturers, exporters, distributors and traders.
click here to find a list of Antox QT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Antox QT DMF (Drug Master File) is a document detailing the whole manufacturing process of Antox QT active pharmaceutical ingredient (API) in detail. Different forms of Antox QT DMFs exist exist since differing nations have different regulations, such as Antox QT USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Antox QT DMF submitted to regulatory agencies in the US is known as a USDMF. Antox QT USDMF includes data on Antox QT's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Antox QT USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Antox QT suppliers with USDMF on PharmaCompass.
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