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up and up nicotine polacrilex - 11673-206-25 - (Nicotine Polacrilex)

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Drug Information of up and up nicotine polacrilex

Product NDC: 11673-206
Proprietary Name: up and up nicotine polacrilex
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 polacrilex

Product NDC: 11673-206
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078325
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of up and up nicotine polacrilex

Package NDC: 11673-206-25
Package Description: 11 BLISTER PACK in 1 CARTON (11673-206-25) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of up and up nicotine polacrilex

NDC Code 11673-206-25
Proprietary Name up and up nicotine polacrilex
Package Description 11 BLISTER PACK in 1 CARTON (11673-206-25) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 11673-206
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20111006
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 polacrilex


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