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Up and Up Nicotine - 11673-352-78 - (Nicotine Polacrilex)

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Drug Information of Up and Up Nicotine

Product NDC: 11673-352
Proprietary Name: Up and Up Nicotine
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 Up and Up Nicotine

Product NDC: 11673-352
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078547
Marketing Category: ANDA
Start Marketing Date: 20110210

Package Information of Up and Up Nicotine

Package NDC: 11673-352-78
Package Description: 10 BLISTER PACK in 1 CARTON (11673-352-78) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of Up and Up Nicotine

NDC Code 11673-352-78
Proprietary Name Up and Up Nicotine
Package Description 10 BLISTER PACK in 1 CARTON (11673-352-78) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 11673-352
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20110210
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Up and Up Nicotine


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