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Lansoprazole

NDC 69842-507 · HUMAN OTC DRUG · TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE

Labeler / ManufacturerCVS Pharmacy
Marketing categoryNew Drug Application (innovator) · App NDA208025
Dosage form / routeTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20171202
Package count1

External sources

Source: openFDA. Public-domain (CC0).