# Pantoprazole Sodium

NDC: 62175-618
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20110120

FDA application: ANDA078281

## Active ingredients

- PANTOPRAZOLE SODIUM: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62175-618"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62175-618
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7705bf6-e473-4b9c-bb5d-57e26ffe7b97