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 1Blank
01 1OXYBUTYNIN
02 3OXYBUTYNIN BASE
01 1France
02 1Ireland
03 1Japan
04 1Blank
01 2Active
02 2Inactive
01 1Complete
02 3Blank
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
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, 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.
A Lenditro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lenditro, including repackagers and relabelers. The FDA regulates Lenditro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lenditro 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 Lenditro manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lenditro supplier is an individual or a company that provides Lenditro active pharmaceutical ingredient (API) or Lenditro finished formulations upon request. The Lenditro suppliers may include Lenditro API manufacturers, exporters, distributors and traders.
click here to find a list of Lenditro suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Lenditro DMF (Drug Master File) is a document detailing the whole manufacturing process of Lenditro active pharmaceutical ingredient (API) in detail. Different forms of Lenditro DMFs exist exist since differing nations have different regulations, such as Lenditro USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lenditro DMF submitted to regulatory agencies in the US is known as a USDMF. Lenditro USDMF includes data on Lenditro's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lenditro USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lenditro suppliers with USDMF on PharmaCompass.
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