GELNIQUE - 54868-6171-0 - (oxybutynin chloride)

Alphabetical Index


Drug Information of GELNIQUE

Product NDC: 54868-6171
Proprietary Name: GELNIQUE
Non Proprietary Name: oxybutynin chloride
Active Ingredient(s): 100    mg/g & nbsp;   oxybutynin chloride
Administration Route(s): TRANSDERMAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of GELNIQUE

Product NDC: 54868-6171
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022204
Marketing Category: NDA
Start Marketing Date: 20100915

Package Information of GELNIQUE

Package NDC: 54868-6171-0
Package Description: 30 PACKET in 1 CARTON (54868-6171-0) > 1 g in 1 PACKET

NDC Information of GELNIQUE

NDC Code 54868-6171-0
Proprietary Name GELNIQUE
Package Description 30 PACKET in 1 CARTON (54868-6171-0) > 1 g in 1 PACKET
Product NDC 54868-6171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name GEL
Route Name TRANSDERMAL
Start Marketing Date 20100915
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 100
Strength Unit mg/g
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of GELNIQUE


General Information