01 2Blank
01 1BUPHENINE HCL (NYLIDRIN)
02 1NYLIDRIN HCL
01 2Blank
01 2Inactive
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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
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
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 Buphenine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buphenine hydrochloride, including repackagers and relabelers. The FDA regulates Buphenine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buphenine hydrochloride 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 Buphenine hydrochloride supplier is an individual or a company that provides Buphenine hydrochloride active pharmaceutical ingredient (API) or Buphenine hydrochloride finished formulations upon request. The Buphenine hydrochloride suppliers may include Buphenine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Buphenine hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Buphenine hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Buphenine hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Buphenine hydrochloride DMFs exist exist since differing nations have different regulations, such as Buphenine hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Buphenine hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Buphenine hydrochloride USDMF includes data on Buphenine hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Buphenine hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Buphenine hydrochloride suppliers with USDMF on PharmaCompass.
