# Lansoprazole

NDC: 71335-2957
Generic name: lansoprazole
Labeler / Manufacturer: Bryant Ranch Prepack
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:"71335-2957"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2957
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7a3aa37-9c9b-43fe-92be-6e0fdc8d1c92
