Nicorette - 0135-0466-07 - (nicotine polacrilex)

Alphabetical Index


Drug Information of Nicorette

Product NDC: 0135-0466
Proprietary Name: Nicorette
Non Proprietary Name: nicotine polacrilex
Active Ingredient(s): 2    mg/1 & nbsp;   nicotine polacrilex
Administration Route(s): ORAL
Dosage Form(s): GUM, CHEWING
Coding System: National Drug Codes(NDC)

Labeler Information of Nicorette

Product NDC: 0135-0466
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA018612
Marketing Category: NDA
Start Marketing Date: 20090629

Package Information of Nicorette

Package NDC: 0135-0466-07
Package Description: 1 BLISTER PACK in 1 CARTON (0135-0466-07) > 40 GUM, CHEWING in 1 BLISTER PACK

NDC Information of Nicorette

NDC Code 0135-0466-07
Proprietary Name Nicorette
Package Description 1 BLISTER PACK in 1 CARTON (0135-0466-07) > 40 GUM, CHEWING in 1 BLISTER PACK
Product NDC 0135-0466
Product Type Name HUMAN OTC DRUG
Non Proprietary Name nicotine polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20090629
Marketing Category Name NDA
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Nicorette


General Information