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Oxybutynin Chloride - 54868-5742-1 - (Oxybutynin Chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 54868-5742
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 54868-5742
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076702
Marketing Category: ANDA
Start Marketing Date: 20070108

Package Information of Oxybutynin Chloride

Package NDC: 54868-5742-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5742-1)

NDC Information of Oxybutynin Chloride

NDC Code 54868-5742-1
Proprietary Name Oxybutynin Chloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5742-1)
Product NDC 54868-5742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxybutynin Chloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070108
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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