# Lansoprazole

NDC: 68788-4141
Generic name: lansoprazole
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20260812

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:"68788-4141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-4141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7a79feee-2e21-4cd0-a720-c59643764303