Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Seqens
03 1Abbott Laboratories
04 1Actavis Inc
05 1Aurobindo Pharma Limited
06 1CordenPharma
07 2Harman Finochem
08 1Resonance Laboratories Pvt. Ltd
09 1Siegfried AG
10 1THINQ Pharma-CRO PVT Ltd
11 1Wockhardt
12 1Blank
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 : 12840
Submission : 1998-02-02
Status :
Type : II
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : Complete
Rev. Date : 2013-05-09
Pay. Date : 2013-04-30
DMF Number : 6412
Submission : 1986-06-12
Status :
Type : II
14
PharmaCompass offers a list of Oxybutynin Hydrochloride 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 Oxybutynin Hydrochloride manufacturer or Oxybutynin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Oxybutynin Hydrochloride API Price utilized in the formulation of products. Oxybutynin Hydrochloride API Price is not always fixed or binding as the Oxybutynin Hydrochloride Price is obtained through a variety of data sources. The Oxybutynin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxybutynin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybutynin Hydrochloride, including repackagers and relabelers. The FDA regulates Oxybutynin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybutynin 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.
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A Oxybutynin Hydrochloride supplier is an individual or a company that provides Oxybutynin Hydrochloride active pharmaceutical ingredient (API) or Oxybutynin Hydrochloride finished formulations upon request. The Oxybutynin Hydrochloride suppliers may include Oxybutynin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxybutynin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxybutynin Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxybutynin Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Oxybutynin Hydrochloride DMFs exist exist since differing nations have different regulations, such as Oxybutynin Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxybutynin Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Oxybutynin Hydrochloride USDMF includes data on Oxybutynin Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxybutynin Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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