# Lansoprazole

NDC: 55111-398
Generic name: lansoprazole
Labeler / Manufacturer: Dr.Reddy's Laboratories Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20101015

FDA application: ANDA091269

## 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:"55111-398"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-398
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82174fcc-1b0f-2068-7fc4-db335b43b5e2