01 1S D Fine Chem Limited
01 1SODIUM HYDROXIDE PELLETS BP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28719
Submission : 2014-10-03
Status : Active
Type : IV
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A Aetznatron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aetznatron, including repackagers and relabelers. The FDA regulates Aetznatron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aetznatron 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 Aetznatron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Aetznatron supplier is an individual or a company that provides Aetznatron active pharmaceutical ingredient (API) or Aetznatron finished formulations upon request. The Aetznatron suppliers may include Aetznatron API manufacturers, exporters, distributors and traders.
click here to find a list of Aetznatron suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Aetznatron DMF (Drug Master File) is a document detailing the whole manufacturing process of Aetznatron active pharmaceutical ingredient (API) in detail. Different forms of Aetznatron DMFs exist exist since differing nations have different regulations, such as Aetznatron USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aetznatron DMF submitted to regulatory agencies in the US is known as a USDMF. Aetznatron USDMF includes data on Aetznatron's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aetznatron USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aetznatron suppliers with USDMF on PharmaCompass.
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