# Lansoprazole

NDC: 37808-934
Generic name: Lansoprazole
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220412

FDA application: ANDA202194

## 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:"37808-934"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-934
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e15401b-6cea-4687-8c34-4412734caaac