# Lansoprazole

NDC: 69842-755
Generic name: Lansoprazole
Labeler / Manufacturer: CVS Pharmacy
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190331
Marketing ended: 20261231
FDA application: ANDA203187

## Active ingredients

- LANSOPRAZOLE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69842-755"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69842-755
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d52b26e2-3d2a-4067-a28b-8697f865f582