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01 1BUPHENINE HCL (NYLIDRIN)
02 1NYLIDRIN HCL
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01 2Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1703
Submission : 1970-12-30
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5491
Submission : 1984-07-31
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
12
PharmaCompass offers a list of Buphenine hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Buphenine hydrochloride manufacturer or Buphenine hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Buphenine hydrochloride manufacturer or Buphenine hydrochloride supplier.
A Nylidrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nylidrin, including repackagers and relabelers. The FDA regulates Nylidrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nylidrin 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 Nylidrin supplier is an individual or a company that provides Nylidrin active pharmaceutical ingredient (API) or Nylidrin finished formulations upon request. The Nylidrin suppliers may include Nylidrin API manufacturers, exporters, distributors and traders.
click here to find a list of Nylidrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Nylidrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Nylidrin active pharmaceutical ingredient (API) in detail. Different forms of Nylidrin DMFs exist exist since differing nations have different regulations, such as Nylidrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nylidrin DMF submitted to regulatory agencies in the US is known as a USDMF. Nylidrin USDMF includes data on Nylidrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nylidrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nylidrin suppliers with USDMF on PharmaCompass.
