FDA NDC Directory · JSON-LD · Markdown

Lansoprazole

NDC 37808-934 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA202194
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20220412
Package count2

External sources

Source: openFDA. Public-domain (CC0).