# Pantoprazole Sodium

NDC: 72603-746
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260301

FDA application: ANDA202038

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-746"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-746
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6637d90b-b268-4a5f-ab5b-885f2d5f0d4b