01 1Suven Pharmaceuticals
01 1DANOFLOXACIN MESYLATE
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36905
Submission : 2022-03-19
Status : Active
Type : II
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A Advocid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Advocid, including repackagers and relabelers. The FDA regulates Advocid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Advocid 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 Advocid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Advocid supplier is an individual or a company that provides Advocid active pharmaceutical ingredient (API) or Advocid finished formulations upon request. The Advocid suppliers may include Advocid API manufacturers, exporters, distributors and traders.
click here to find a list of Advocid suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Advocid DMF (Drug Master File) is a document detailing the whole manufacturing process of Advocid active pharmaceutical ingredient (API) in detail. Different forms of Advocid DMFs exist exist since differing nations have different regulations, such as Advocid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Advocid DMF submitted to regulatory agencies in the US is known as a USDMF. Advocid USDMF includes data on Advocid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Advocid USDMF is kept confidential to protect the manufacturer’s intellectual property.
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