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Lansoprazole

NDC 55111-398 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic namelansoprazole
Labeler / ManufacturerDr.Reddy's Laboratories Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA091269
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20101015
Package count6

External sources

Source: openFDA. Public-domain (CC0).