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OXYBUTYNIN CHLORIDE - 0093-5206-01 - (OXYBUTYNIN CHLORIDE)

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Drug Information of OXYBUTYNIN CHLORIDE

Product NDC: 0093-5206
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of OXYBUTYNIN CHLORIDE

Product NDC: 0093-5206
Labeler Name: TEVA Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076745
Marketing Category: ANDA
Start Marketing Date: 20070511

Package Information of OXYBUTYNIN CHLORIDE

Package NDC: 0093-5206-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5206-01)

NDC Information of OXYBUTYNIN CHLORIDE

NDC Code 0093-5206-01
Proprietary Name OXYBUTYNIN CHLORIDE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5206-01)
Product NDC 0093-5206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYBUTYNIN CHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070511
Marketing Category Name ANDA
Labeler Name TEVA Pharmaceuticals USA 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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