# Pantoprazole Sodium

NDC: 25021-751
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Sagent Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220715

FDA application: ANDA204400

## 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:"25021-751"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25021-751
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c39be14b-e881-4586-b77e-4747db494954