Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1Seqens
02 1Actavis Inc
03 1Juzen Chemical Corporation
04 1Siegfried AG
05 1Blank
01 1OXYBUTYNIN
02 4OXYBUTYNIN BASE
01 1France
02 1Ireland
03 1Japan
04 1Switzerland
05 1Blank
01 3Active
02 2Inactive
01 1Complete
02 4Blank
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-04
Pay. Date : 2013-08-21
DMF Number : 13084
Submission : 1998-07-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26077
Submission : 2012-06-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14071
Submission : 1999-03-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11947
Submission : 1996-04-26
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11478
Submission : 1995-04-27
Status : Inactive
Type : II
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PharmaCompass offers a list of Oxybutynin 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 manufacturer or Oxybutynin supplier for your needs.
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PharmaCompass also assists you with knowing the Oxybutynin API Price utilized in the formulation of products. Oxybutynin API Price is not always fixed or binding as the Oxybutynin Price is obtained through a variety of data sources. The Oxybutynin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A O222 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of O222, including repackagers and relabelers. The FDA regulates O222 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. O222 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 O222 supplier is an individual or a company that provides O222 active pharmaceutical ingredient (API) or O222 finished formulations upon request. The O222 suppliers may include O222 API manufacturers, exporters, distributors and traders.
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A O222 DMF (Drug Master File) is a document detailing the whole manufacturing process of O222 active pharmaceutical ingredient (API) in detail. Different forms of O222 DMFs exist exist since differing nations have different regulations, such as O222 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A O222 DMF submitted to regulatory agencies in the US is known as a USDMF. O222 USDMF includes data on O222's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The O222 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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