FDA NDC Directory · JSON-LD · Markdown

Nicotine

NDC 63739-371 · HUMAN OTC DRUG · GUM, CHEWING

Generic namenicotine polacrilex
Labeler / ManufacturerMcKesson Corporation dba SKY Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA074507
Dosage form / routeGUM, CHEWING · ORAL
Active ingredientsNICOTINE (2 mg/1)
Marketing started20200427
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).