01 2Bayer AG
02 1Medimpex
03 1Steroid SpA
04 1Blank
01 1NANDROLONE PHENPROPIONATE
02 1NANDROLONE PHENPROPIONATE USP
03 1NANDROLONE PHENPROPIONATE,17 B-(3-PHENYLPROPIONYLOXY-)4-ESTREN-3-ONE
04 2NANDROLONE PHENYLPROPIONATE
01 2Germany
02 1Italy
03 1United Kingdom
04 1Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4482
Submission : 1982-01-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4406
Submission : 1982-01-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4010
Submission : 1980-11-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6379
Submission : 1986-06-17
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3225
Submission : 1978-05-25
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
71
PharmaCompass offers a list of Nandrolone Phenpropionate 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 Nandrolone Phenpropionate manufacturer or Nandrolone Phenpropionate supplier for your needs.
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PharmaCompass also assists you with knowing the Nandrolone Phenpropionate API Price utilized in the formulation of products. Nandrolone Phenpropionate API Price is not always fixed or binding as the Nandrolone Phenpropionate Price is obtained through a variety of data sources. The Nandrolone Phenpropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_3353 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3353, including repackagers and relabelers. The FDA regulates DSSTox_CID_3353 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3353 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_CID_3353 supplier is an individual or a company that provides DSSTox_CID_3353 active pharmaceutical ingredient (API) or DSSTox_CID_3353 finished formulations upon request. The DSSTox_CID_3353 suppliers may include DSSTox_CID_3353 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3353 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_3353 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_3353 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_3353 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_3353 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSSTox_CID_3353 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_3353 USDMF includes data on DSSTox_CID_3353's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_3353 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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