# Pantoprazole Sodium

NDC: 51655-075
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220927

FDA application: ANDA202038

## Active ingredients

- PANTOPRAZOLE SODIUM: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-075"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-075
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2a1af50-a051-3e55-e053-2a95a90a9184