Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
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01 1Seqens
02 1Actavis Inc
03 1Juzen Chemical Corporation
04 1Siegfried AG
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01 1OXYBUTYNIN
02 4OXYBUTYNIN BASE
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01 1France
02 1Ireland
03 1Japan
04 1Switzerland
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01 3Active
02 2Inactive
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxybutynin manufacturer or Oxybutynin supplier.
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 Driptane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Driptane, including repackagers and relabelers. The FDA regulates Driptane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Driptane 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 Driptane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Driptane supplier is an individual or a company that provides Driptane active pharmaceutical ingredient (API) or Driptane finished formulations upon request. The Driptane suppliers may include Driptane API manufacturers, exporters, distributors and traders.
click here to find a list of Driptane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Driptane DMF (Drug Master File) is a document detailing the whole manufacturing process of Driptane active pharmaceutical ingredient (API) in detail. Different forms of Driptane DMFs exist exist since differing nations have different regulations, such as Driptane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Driptane DMF submitted to regulatory agencies in the US is known as a USDMF. Driptane USDMF includes data on Driptane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Driptane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Driptane suppliers with USDMF on PharmaCompass.
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