01 2Peninsula Laboratories
01 1DYNORPHIN A (1-13, PORCINE)
02 1DYNORPHIN A 1-10 AMIDE
01 2U.S.A
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7172
Submission : 1987-09-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8339
Submission : 1989-12-19
Status : Inactive
Type : II
A Dynorphin A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dynorphin A, including repackagers and relabelers. The FDA regulates Dynorphin A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dynorphin A 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 Dynorphin A supplier is an individual or a company that provides Dynorphin A active pharmaceutical ingredient (API) or Dynorphin A finished formulations upon request. The Dynorphin A suppliers may include Dynorphin A API manufacturers, exporters, distributors and traders.
click here to find a list of Dynorphin A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dynorphin A DMF (Drug Master File) is a document detailing the whole manufacturing process of Dynorphin A active pharmaceutical ingredient (API) in detail. Different forms of Dynorphin A DMFs exist exist since differing nations have different regulations, such as Dynorphin A USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dynorphin A DMF submitted to regulatory agencies in the US is known as a USDMF. Dynorphin A USDMF includes data on Dynorphin A's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dynorphin A USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dynorphin A suppliers with USDMF on PharmaCompass.
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