01 1Cody Laboratories, Inc.
02 3Blank
01 1PHENTERMINE BASE & HCL
02 1PHENTERMINE RESIN - API
03 1PHENTERMINE RESINATE
04 1PHENTERMINE RESINATE (BULK FORM)
01 1U.S.A
02 3Blank
01 4Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20135
Submission : 2007-01-11
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5088
Submission : 1983-08-15
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 : 3717
Submission : 1980-01-28
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 : 2971
Submission : 1977-06-27
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Fentermina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fentermina, including repackagers and relabelers. The FDA regulates Fentermina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fentermina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Fentermina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fentermina supplier is an individual or a company that provides Fentermina active pharmaceutical ingredient (API) or Fentermina finished formulations upon request. The Fentermina suppliers may include Fentermina API manufacturers, exporters, distributors and traders.
click here to find a list of Fentermina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fentermina DMF (Drug Master File) is a document detailing the whole manufacturing process of Fentermina active pharmaceutical ingredient (API) in detail. Different forms of Fentermina DMFs exist exist since differing nations have different regulations, such as Fentermina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fentermina DMF submitted to regulatory agencies in the US is known as a USDMF. Fentermina USDMF includes data on Fentermina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fentermina USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fentermina suppliers with USDMF on PharmaCompass.
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