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Oxybutynin Chloride - 50111-456-01 - (Oxybutynin Chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 50111-456
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: 50111-456
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071655
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Oxybutynin Chloride

Package NDC: 50111-456-01
Package Description: 100 TABLET in 1 BOTTLE (50111-456-01)

NDC Information of Oxybutynin Chloride

NDC Code 50111-456-01
Proprietary Name Oxybutynin Chloride
Package Description 100 TABLET in 1 BOTTLE (50111-456-01)
Product NDC 50111-456
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxybutynin Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Pliva Inc.
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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