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In control nicotine - 37808-029-60 - (Nicotine Polacrilex)

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Drug Information of In control nicotine

Product NDC: 37808-029
Proprietary Name: In control 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 In control nicotine

Product NDC: 37808-029
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076775
Marketing Category: ANDA
Start Marketing Date: 20050606

Package Information of In control nicotine

Package NDC: 37808-029-60
Package Description: 2 BLISTER PACK in 1 CARTON (37808-029-60) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of In control nicotine

NDC Code 37808-029-60
Proprietary Name In control nicotine
Package Description 2 BLISTER PACK in 1 CARTON (37808-029-60) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 37808-029
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20050606
Marketing Category Name ANDA
Labeler Name H E B
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of In control nicotine


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