01 1Emeishan Hongsheng Pharmaceutical
01 1PIDOTIMOD
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42167
Submission : 2025-06-26
Status : Active
Type : II
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A Adimod manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adimod, including repackagers and relabelers. The FDA regulates Adimod manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adimod 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 Adimod manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Adimod supplier is an individual or a company that provides Adimod active pharmaceutical ingredient (API) or Adimod finished formulations upon request. The Adimod suppliers may include Adimod API manufacturers, exporters, distributors and traders.
click here to find a list of Adimod suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Adimod DMF (Drug Master File) is a document detailing the whole manufacturing process of Adimod active pharmaceutical ingredient (API) in detail. Different forms of Adimod DMFs exist exist since differing nations have different regulations, such as Adimod USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Adimod DMF submitted to regulatory agencies in the US is known as a USDMF. Adimod USDMF includes data on Adimod's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Adimod USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Adimod suppliers with USDMF on PharmaCompass.
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