FDA NDC Directory · JSON-LD · Markdown

lansoprazole

NDC 63629-7552 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA202366
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsLANSOPRAZOLE (30 mg/1)
Marketing started20130823
Package count9

External sources

Source: openFDA. Public-domain (CC0).