FDA NDC Directory · JSON-LD · Markdown

LANSOPRAZOLE

NDC 72288-672 · HUMAN OTC DRUG · TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE

Generic nameLansoprazole
Labeler / ManufacturerAmazon.com Services LLC
Marketing categoryNew Drug Application (innovator) · App NDA208025
Dosage form / routeTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20260812
Package count1

External sources

Source: openFDA. Public-domain (CC0).