# Lansoprazole

NDC: 0378-8015
Generic name: lansoprazole
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20091110

FDA application: ANDA090763

## Active ingredients

- LANSOPRAZOLE: 15 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-8015"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-8015
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8fa7401-907f-41b6-a2e1-f4bc214f2cdf