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sunmark nicotine - 49348-573-36 - (Nicotine Polacrilex)

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Drug Information of sunmark nicotine

Product NDC: 49348-573
Proprietary Name: sunmark 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 sunmark nicotine

Product NDC: 49348-573
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076775
Marketing Category: ANDA
Start Marketing Date: 20050618

Package Information of sunmark nicotine

Package NDC: 49348-573-36
Package Description: 11 BLISTER PACK in 1 CARTON (49348-573-36) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of sunmark nicotine

NDC Code 49348-573-36
Proprietary Name sunmark nicotine
Package Description 11 BLISTER PACK in 1 CARTON (49348-573-36) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 49348-573
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20050618
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of sunmark nicotine


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