# Pantoprazole sodium

NDC: 71839-122
Generic name: Pantoprazole sodium
Labeler / Manufacturer: BE Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220525

FDA application: ANDA216171

## 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:"71839-122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71839-122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52d5bc28-66df-43aa-bb1a-8ac4a2a7f693