# PANTOPRAZOLE SODIUM

NDC: 0338-9646
Generic name: Pantoprazole Sodium in 0.9% Sodium Chloride
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240214

FDA application: NDA217512

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-9646"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-9646
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a476e063-9450-4793-9a22-16b0a0a61cd0