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kirkland signature quit 2 - 63981-029-01 - (Nicotine Polacrilex)

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Drug Information of kirkland signature quit 2

Product NDC: 63981-029
Proprietary Name: kirkland signature quit 2
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 kirkland signature quit 2

Product NDC: 63981-029
Labeler Name: Costco Wholesale Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076775
Marketing Category: ANDA
Start Marketing Date: 20120515

Package Information of kirkland signature quit 2

Package NDC: 63981-029-01
Package Description: 2 CARTON in 1 CARTON (63981-029-01) > 19 BLISTER PACK in 1 CARTON (63981-029-56) > 10 GUM, CHEWING in 1 BLISTER PACK

NDC Information of kirkland signature quit 2

NDC Code 63981-029-01
Proprietary Name kirkland signature quit 2
Package Description 2 CARTON in 1 CARTON (63981-029-01) > 19 BLISTER PACK in 1 CARTON (63981-029-56) > 10 GUM, CHEWING in 1 BLISTER PACK
Product NDC 63981-029
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Nicotine Polacrilex
Dosage Form Name GUM, CHEWING
Route Name ORAL
Start Marketing Date 20120515
Marketing Category Name ANDA
Labeler Name Costco Wholesale Company
Substance Name NICOTINE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of kirkland signature quit 2


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