FDA NDC Directory · JSON-LD · Markdown

LANSOPRAZOLE

NDC 72288-827 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Generic nameLansoprazole
Labeler / ManufacturerAmazon.com Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202319
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20260709
Package count1

External sources

Source: openFDA. Public-domain (CC0).