Nicorelief - 0904-5736-51 - (Nicotine Polacrilex)

Alphabetical Index


Drug Information of Nicorelief

Product NDC: 0904-5736
Proprietary Name: Nicorelief
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 Nicorelief

Product NDC: 0904-5736
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078325
Marketing Category: ANDA
Start Marketing Date: 20050412

Package Information of Nicorelief

Package NDC: 0904-5736-51
Package Description: 5 BLISTER PACK in 1 CARTON (0904-5736-51) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of Nicorelief

NDC Code 0904-5736-51
Proprietary Name Nicorelief
Package Description 5 BLISTER PACK in 1 CARTON (0904-5736-51) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 0904-5736
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20050412
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Nicorelief


General Information