# Pantoprazole Sodium

NDC: 72572-553
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Civica, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250601

FDA application: NDA209463

## 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:"72572-553"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-553
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c857dc41-7b47-4f26-a9f5-d76eb82b44ee