ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
01 1ChemWerth Inc
02 1Sanofi
03 1Abbott Laboratories
04 1CHEMSYN CHEMICAL CORPORATION
05 1Gilead Sciences
06 1Hainan Poly Pharm
07 1Huhtamaki
08 1Recordati
09 1Siegfried AG
10 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 : 8856
Submission : 1990-11-20
Status :
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12528
Submission : 1997-05-30
Status :
Type : II
A Dobutamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dobutamine Hydrochloride, including repackagers and relabelers. The FDA regulates Dobutamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dobutamine Hydrochloride 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 Dobutamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dobutamine Hydrochloride supplier is an individual or a company that provides Dobutamine Hydrochloride active pharmaceutical ingredient (API) or Dobutamine Hydrochloride finished formulations upon request. The Dobutamine Hydrochloride suppliers may include Dobutamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dobutamine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dobutamine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Dobutamine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Dobutamine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Dobutamine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dobutamine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Dobutamine Hydrochloride USDMF includes data on Dobutamine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dobutamine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dobutamine Hydrochloride suppliers with USDMF on PharmaCompass.
We have 9 companies offering Dobutamine Hydrochloride
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