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In Control Nicotine - 37808-532-78 - (Nicotine Polacrilex)

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Drug Information of In Control Nicotine

Product NDC: 37808-532
Proprietary Name: In Control Nicotine
Non Proprietary Name: Nicotine Polacrilex
Active Ingredient(s): 4    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: 37808-532
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076779
Marketing Category: ANDA
Start Marketing Date: 20061013

Package Information of In Control Nicotine

Package NDC: 37808-532-78
Package Description: 10 BLISTER PACK in 1 CARTON (37808-532-78) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of In Control Nicotine

NDC Code 37808-532-78
Proprietary Name In Control Nicotine
Package Description 10 BLISTER PACK in 1 CARTON (37808-532-78) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 37808-532
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20061013
Marketing Category Name ANDA
Labeler Name H E B
Substance Name NICOTINE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of In Control Nicotine


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