# Lansoprazole

NDC: 46122-744
Generic name: Lansoprazole
Labeler / Manufacturer: AMERISOURCEBERGEN DRUG CORPORATION
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220412

FDA application: ANDA202194

## 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:"46122-744"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-744
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=accb92e8-dd14-b87b-c20a-6c4803815bc2