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berkley and jensen nicotine - 68391-029-78 - (Nicotine Polacrilex)

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Drug Information of berkley and jensen nicotine

Product NDC: 68391-029
Proprietary Name: berkley and jensen 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 berkley and jensen nicotine

Product NDC: 68391-029
Labeler Name: BJWC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076775
Marketing Category: ANDA
Start Marketing Date: 20060119

Package Information of berkley and jensen nicotine

Package NDC: 68391-029-78
Package Description: 10 BLISTER PACK in 1 CARTON (68391-029-78) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of berkley and jensen nicotine

NDC Code 68391-029-78
Proprietary Name berkley and jensen nicotine
Package Description 10 BLISTER PACK in 1 CARTON (68391-029-78) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 68391-029
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20060119
Marketing Category Name ANDA
Labeler Name BJWC
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of berkley and jensen nicotine


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