Nicotine

Product NDC
59726-913
Type
HUMAN OTC DRUG
Nonproprietary name
Nicotine Polacrilex
Dosage form
GUM, CHEWING
Route
ORAL
Labeler
P & L Development, LLC
Application
ANDA079038
Marketing category
ANDA
Substance
NICOTINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
59726-913-16160 BLISTER PACK in 1 CARTON (59726-913-16) / 1 GUM, CHEWING in 1 BLISTER PACK2024-03-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Nicotine 4 mg Fruit Coated USP GumP & L Development, LLC2026-02-26HUMAN OTC DRUG LABEL4