01 1Celanese
02 1GSK
03 1Kyowa Hakko Bio
04 1Recordati
05 1Siegfried AG
06 1Zambon Switzerland
07 1Blank
01 1DOPAMIN HCL
02 1DOPAMINE HCL USP XX
03 1DOPAMINE HCL, BULK DRUG SUBSTANCE
04 1DOPAMINE HCl
05 2DOPAMINE HYDROCHLORIDE
06 1L-DOPAMINE HYDROCHLORIDE (3-HYDROXYTYRAMINE HYDROCHLORIDE )
01 1Italy
02 1Japan
03 2Switzerland
04 1U.S.A
05 1United Kingdom
06 1Blank
01 2Active
02 5Inactive
01 1Complete
02 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4415
Submission : 1982-01-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2453
Submission : 1975-05-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3060
Submission : 1977-11-22
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-03-30
Pay. Date : 2014-05-30
DMF Number : 5134
Submission : 1983-06-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3116
Submission : 1977-12-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5788
Submission : 1985-03-29
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3165
Submission : 1978-02-22
Status : Inactive
Type : II
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A CAS-62-31-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-62-31-7, including repackagers and relabelers. The FDA regulates CAS-62-31-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-62-31-7 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 CAS-62-31-7 supplier is an individual or a company that provides CAS-62-31-7 active pharmaceutical ingredient (API) or CAS-62-31-7 finished formulations upon request. The CAS-62-31-7 suppliers may include CAS-62-31-7 API manufacturers, exporters, distributors and traders.
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A CAS-62-31-7 DMF (Drug Master File) is a document detailing the whole manufacturing process of CAS-62-31-7 active pharmaceutical ingredient (API) in detail. Different forms of CAS-62-31-7 DMFs exist exist since differing nations have different regulations, such as CAS-62-31-7 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CAS-62-31-7 DMF submitted to regulatory agencies in the US is known as a USDMF. CAS-62-31-7 USDMF includes data on CAS-62-31-7's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CAS-62-31-7 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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