# Lansoprazole

NDC: 67877-274
Generic name: Lansoprazole
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190120

FDA application: ANDA207394

## 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:"67877-274"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-274
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e246e79-2737-4cbb-ad5d-4e76893da3be