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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxybutynin Hydrochloride manufacturer or Oxybutynin Hydrochloride supplier.
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 Oxibutinina hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxibutinina hydrochloride, including repackagers and relabelers. The FDA regulates Oxibutinina hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxibutinina 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 Oxibutinina hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxibutinina hydrochloride supplier is an individual or a company that provides Oxibutinina hydrochloride active pharmaceutical ingredient (API) or Oxibutinina hydrochloride finished formulations upon request. The Oxibutinina hydrochloride suppliers may include Oxibutinina hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxibutinina hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxibutinina hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxibutinina hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Oxibutinina hydrochloride DMFs exist exist since differing nations have different regulations, such as Oxibutinina hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxibutinina hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Oxibutinina hydrochloride USDMF includes data on Oxibutinina hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxibutinina hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxibutinina hydrochloride suppliers with USDMF on PharmaCompass.
We have 11 companies offering Oxibutinina hydrochloride
Get in contact with the supplier of your choice:
