Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1Rusan Pharma
02 1Lonza Group
03 1ScinoPharm Taiwan Ltd
01 1DL-2-(DIFLUOROMETHYL) ORNITHINE MONOHYDROCHLORIDE MONOHYDRATE
02 1EFLORNITHINE HYDROCHLORIDE
03 1EFLORNITHINE HYDROCHLORIDE MONOHYDRATE
01 1India
02 1Switzerland
03 1Taiwan
01 2Active
02 1Inactive
01 3Blank
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31780
Submission : 2017-06-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11932
Submission : 1996-04-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18509
Submission : 2005-07-12
Status : Active
Type : II
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PharmaCompass offers a list of Eflornithine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Eflornithine Hydrochloride manufacturer or Eflornithine Hydrochloride supplier for your needs.
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A CCRIS 5805 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCRIS 5805, including repackagers and relabelers. The FDA regulates CCRIS 5805 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCRIS 5805 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 CCRIS 5805 supplier is an individual or a company that provides CCRIS 5805 active pharmaceutical ingredient (API) or CCRIS 5805 finished formulations upon request. The CCRIS 5805 suppliers may include CCRIS 5805 API manufacturers, exporters, distributors and traders.
click here to find a list of CCRIS 5805 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A CCRIS 5805 DMF (Drug Master File) is a document detailing the whole manufacturing process of CCRIS 5805 active pharmaceutical ingredient (API) in detail. Different forms of CCRIS 5805 DMFs exist exist since differing nations have different regulations, such as CCRIS 5805 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CCRIS 5805 DMF submitted to regulatory agencies in the US is known as a USDMF. CCRIS 5805 USDMF includes data on CCRIS 5805's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CCRIS 5805 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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