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Oxybutynin Chloride - 63629-1354-1 - (oxybutynin chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 63629-1354
Proprietary Name: Oxybutynin Chloride
Non Proprietary Name: oxybutynin chloride
Active Ingredient(s): 5    mg/1 & nbsp;   oxybutynin chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 63629-1354
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075079
Marketing Category: ANDA
Start Marketing Date: 19971031

Package Information of Oxybutynin Chloride

Package NDC: 63629-1354-1
Package Description: 30 TABLET in 1 BOTTLE (63629-1354-1)

NDC Information of Oxybutynin Chloride

NDC Code 63629-1354-1
Proprietary Name Oxybutynin Chloride
Package Description 30 TABLET in 1 BOTTLE (63629-1354-1)
Product NDC 63629-1354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19971031
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Oxybutynin Chloride


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