# PANTOPRAZOLE SODIUM I.V.

NDC: 0781-3480
Generic name: PANTOPRAZOLE SODIUM
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260126

FDA application: ANDA209524

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3480"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3480
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22b71a1d-87f8-43ba-b53d-53ca3f70c63e