GELNIQUE - 52544-084-30 - (oxybutynin chloride)

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Drug Information of GELNIQUE

Product NDC: 52544-084
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: 52544-084
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022204
Marketing Category: NDA
Start Marketing Date: 20090515

Package Information of GELNIQUE

Package NDC: 52544-084-30
Package Description: 30 PACKET in 1 CARTON (52544-084-30) > 1 g in 1 PACKET

NDC Information of GELNIQUE

NDC Code 52544-084-30
Proprietary Name GELNIQUE
Package Description 30 PACKET in 1 CARTON (52544-084-30) > 1 g in 1 PACKET
Product NDC 52544-084
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name GEL
Route Name TRANSDERMAL
Start Marketing Date 20090515
Marketing Category Name NDA
Labeler Name Watson Pharma, 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