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01 1Zhejiang Jiuzhou Pharmaceutical
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01 1MAP(VERSION NO.:1) (4R,5R,6S)-3-[(DIPHENOXYPHOSPHINYL)OXYL-6-[(1R)-1-HYDROXYETHYL]-7-OXO-1-AZABICYCLO[3.2.0]HEPT-2-ENE-2-CARBOXYLIC ACID (4-NITROPHENYL) METHYL ESTER
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01 1China
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01 1Active
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26850
Submission : 2013-01-25
Status : Active
Type : II
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A Molport-021-783-041 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Molport-021-783-041, including repackagers and relabelers. The FDA regulates Molport-021-783-041 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Molport-021-783-041 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Molport-021-783-041 supplier is an individual or a company that provides Molport-021-783-041 active pharmaceutical ingredient (API) or Molport-021-783-041 finished formulations upon request. The Molport-021-783-041 suppliers may include Molport-021-783-041 API manufacturers, exporters, distributors and traders.
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A Molport-021-783-041 DMF (Drug Master File) is a document detailing the whole manufacturing process of Molport-021-783-041 active pharmaceutical ingredient (API) in detail. Different forms of Molport-021-783-041 DMFs exist exist since differing nations have different regulations, such as Molport-021-783-041 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Molport-021-783-041 DMF submitted to regulatory agencies in the US is known as a USDMF. Molport-021-783-041 USDMF includes data on Molport-021-783-041's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Molport-021-783-041 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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