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
73
PharmaCompass offers a list of Phentermine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Phentermine manufacturer or Phentermine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phentermine manufacturer or Phentermine supplier.
PharmaCompass also assists you with knowing the Phentermine API Price utilized in the formulation of products. Phentermine API Price is not always fixed or binding as the Phentermine Price is obtained through a variety of data sources. The Phentermine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C07438 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07438, including repackagers and relabelers. The FDA regulates C07438 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07438 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 C07438 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C07438 supplier is an individual or a company that provides C07438 active pharmaceutical ingredient (API) or C07438 finished formulations upon request. The C07438 suppliers may include C07438 API manufacturers, exporters, distributors and traders.
click here to find a list of C07438 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C07438 DMF (Drug Master File) is a document detailing the whole manufacturing process of C07438 active pharmaceutical ingredient (API) in detail. Different forms of C07438 DMFs exist exist since differing nations have different regulations, such as C07438 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C07438 DMF submitted to regulatory agencies in the US is known as a USDMF. C07438 USDMF includes data on C07438's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C07438 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of C07438 suppliers with USDMF on PharmaCompass.
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