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Oxybutynin Chloride - 50268-629-13 - (Oxybutynin Chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 50268-629
Proprietary Name: Oxybutynin Chloride
Non Proprietary Name: Oxybutynin Chloride
Active Ingredient(s): 15    mg/1 & nbsp;   Oxybutynin Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 50268-629
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078503
Marketing Category: ANDA
Start Marketing Date: 20120516

Package Information of Oxybutynin Chloride

Package NDC: 50268-629-13
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (50268-629-13)

NDC Information of Oxybutynin Chloride

NDC Code 50268-629-13
Proprietary Name Oxybutynin Chloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (50268-629-13)
Product NDC 50268-629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxybutynin Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120516
Marketing Category Name ANDA
Labeler Name AvPAK
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Oxybutynin Chloride


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