Ditropan - 54868-4835-0 - (oxybutynin chloride)

Alphabetical Index


Drug Information of Ditropan

Product NDC: 54868-4835
Proprietary Name: Ditropan
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 Ditropan

Product NDC: 54868-4835
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020897
Marketing Category: NDA
Start Marketing Date: 20030625

Package Information of Ditropan

Package NDC: 54868-4835-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-4835-0)

NDC Information of Ditropan

NDC Code 54868-4835-0
Proprietary Name Ditropan
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-4835-0)
Product NDC 54868-4835
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030625
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Ditropan


General Information