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Lansoprazole

NDC 69842-755 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerCVS Pharmacy
Marketing categoryAbbreviated NDA (generic) · App ANDA203187
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (15 mg/1)
Marketing started20190331
Marketing ended20261231
Package count3

External sources

Source: openFDA. Public-domain (CC0).