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Lansoprazole

NDC 68788-4141 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Generic namelansoprazole
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090763
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsLANSOPRAZOLE (30 mg/1)
Marketing started20260812
Package count3

External sources

Source: openFDA. Public-domain (CC0).