# Lansoprazole

NDC: 48433-051
Generic name: lansoprazole
Labeler / Manufacturer: Safecor Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20260616

FDA application: ANDA090763

## 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:"48433-051"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=48433-051
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47a8618c-e768-41bf-9116-634b564405d4