ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
01 1ChemWerth Inc
02 1Cambridge Major Laboratories
03 1Epoch Labs
04 1Reliable Biopharmaceutical Corporation
01 1FENOLDOPAM MESYLATE (NON-STERILE BULK DRUG SUBSTANCE)
02 1FENOLDOPAM MESYLATE BULK ACTIVE API
03 1FENOLDOPAM MESYLATE USP
04 1FENOLDOPAM MESYLATE, USP
01 1India
02 1Netherlands
03 2U.S.A
01 2Active
02 2Inactive
01 4Blank
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16582
Submission : 2003-05-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16145
Submission : 2002-09-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19636
Submission : 2006-06-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17248
Submission : 2004-03-22
Status : Inactive
Type : II
A Fenoldopam (mesylate) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenoldopam (mesylate), including repackagers and relabelers. The FDA regulates Fenoldopam (mesylate) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenoldopam (mesylate) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fenoldopam (mesylate) supplier is an individual or a company that provides Fenoldopam (mesylate) active pharmaceutical ingredient (API) or Fenoldopam (mesylate) finished formulations upon request. The Fenoldopam (mesylate) suppliers may include Fenoldopam (mesylate) API manufacturers, exporters, distributors and traders.
click here to find a list of Fenoldopam (mesylate) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fenoldopam (mesylate) DMF (Drug Master File) is a document detailing the whole manufacturing process of Fenoldopam (mesylate) active pharmaceutical ingredient (API) in detail. Different forms of Fenoldopam (mesylate) DMFs exist exist since differing nations have different regulations, such as Fenoldopam (mesylate) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fenoldopam (mesylate) DMF submitted to regulatory agencies in the US is known as a USDMF. Fenoldopam (mesylate) USDMF includes data on Fenoldopam (mesylate)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fenoldopam (mesylate) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fenoldopam (mesylate) suppliers with USDMF on PharmaCompass.
We have 4 companies offering Fenoldopam (mesylate)
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