01 1Gyma Laboratories of America
02 1Midas Pharma
03 1Olon S.p.A
04 2Blank
01 1DIETHYLPROPION HCL
02 1DIETHYLPROPION HYDROCHLORIDE
03 1DIETHYLPROPION-HYDROCHLORIDE
04 2DIETHYLPROPIONE HCL
01 1Germany
02 1Italy
03 1U.S.A
04 2Blank
01 2Active
02 3Inactive
01 1Complete
02 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2142
Submission : 1973-08-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3437
Submission : 1978-11-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-10
Pay. Date : 2013-11-29
DMF Number : 2738
Submission : 1976-08-02
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5158
Submission : 1983-10-03
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 : 2566
Submission : 1975-11-25
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
66
PharmaCompass offers a list of Diethylpropion Hydrochloride 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 Diethylpropion Hydrochloride manufacturer or Diethylpropion Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diethylpropion Hydrochloride manufacturer or Diethylpropion Hydrochloride supplier.
PharmaCompass also assists you with knowing the Diethylpropion Hydrochloride API Price utilized in the formulation of products. Diethylpropion Hydrochloride API Price is not always fixed or binding as the Diethylpropion Hydrochloride Price is obtained through a variety of data sources. The Diethylpropion Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nobesine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nobesine, including repackagers and relabelers. The FDA regulates Nobesine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nobesine 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 Nobesine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nobesine supplier is an individual or a company that provides Nobesine active pharmaceutical ingredient (API) or Nobesine finished formulations upon request. The Nobesine suppliers may include Nobesine API manufacturers, exporters, distributors and traders.
click here to find a list of Nobesine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nobesine DMF (Drug Master File) is a document detailing the whole manufacturing process of Nobesine active pharmaceutical ingredient (API) in detail. Different forms of Nobesine DMFs exist exist since differing nations have different regulations, such as Nobesine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nobesine DMF submitted to regulatory agencies in the US is known as a USDMF. Nobesine USDMF includes data on Nobesine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nobesine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nobesine suppliers with USDMF on PharmaCompass.
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