Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Maithri Drugs
03 1Olon S.p.A
04 3Blank
01 1DEXFENFLURAMINE HYDROCHLORIDE
02 1FENFLURAMINE HYDROCHLORIDE
03 4FENFLURAMINE HYDROCHLORIDE
01 2India
02 1Italy
03 3Blank
01 3Active
02 3Inactive
01 2Complete
02 4Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37321
Submission : 2022-07-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-06-09
Pay. Date : 2021-05-05
DMF Number : 34897
Submission : 2020-05-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-01-22
Pay. Date : 2020-11-05
DMF Number : 35339
Submission : 2020-11-09
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12056
Submission : 1996-07-22
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 : 11946
Submission : 1996-04-25
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 : 10871
Submission : 1994-04-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Fenfluramine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenfluramine Hydrochloride, including repackagers and relabelers. The FDA regulates Fenfluramine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenfluramine 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 Fenfluramine Hydrochloride supplier is an individual or a company that provides Fenfluramine Hydrochloride active pharmaceutical ingredient (API) or Fenfluramine Hydrochloride finished formulations upon request. The Fenfluramine Hydrochloride suppliers may include Fenfluramine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fenfluramine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fenfluramine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Fenfluramine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Fenfluramine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Fenfluramine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fenfluramine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Fenfluramine Hydrochloride USDMF includes data on Fenfluramine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fenfluramine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fenfluramine Hydrochloride suppliers with USDMF on PharmaCompass.
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