# Lansoprazole

NDC: 43598-161
Generic name: Lansoprazole
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20221001

FDA application: ANDA202194

## Active ingredients

- LANSOPRAZOLE: 15 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-161"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-161
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a24acc0b-7770-1087-77bd-048259a5bf72