NICODERM - 0135-0194-01 - (nicotine)

Alphabetical Index


Drug Information of NICODERM

Product NDC: 0135-0194
Proprietary Name: NICODERM
Non Proprietary Name: nicotine
Active Ingredient(s): 21    mg/24h & nbsp;   nicotine
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of NICODERM

Product NDC: 0135-0194
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020165
Marketing Category: NDA
Start Marketing Date: 20110512

Package Information of NICODERM

Package NDC: 0135-0194-01
Package Description: 7 PATCH in 1 CARTON (0135-0194-01) > 24 h in 1 PATCH

NDC Information of NICODERM

NDC Code 0135-0194-01
Proprietary Name NICODERM
Package Description 7 PATCH in 1 CARTON (0135-0194-01) > 24 h in 1 PATCH
Product NDC 0135-0194
Product Type Name HUMAN OTC DRUG
Non Proprietary Name nicotine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20110512
Marketing Category Name NDA
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name NICOTINE
Strength Number 21
Strength Unit mg/24h
Pharmaceutical Classes

Complete Information of NICODERM


General Information