# Lansoprazole DR

NDC: 80425-0174
Generic name: Lansoprazole
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180604

FDA application: ANDA205868

## Active ingredients

- LANSOPRAZOLE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce1a4f32-da65-29d3-e053-2995a90a42ee