# Protonix I.V.

NDC: 0008-4001
Generic name: PANTOPRAZOLE SODIUM
Labeler / Manufacturer: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20130501

FDA application: NDA020988

## 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:"0008-4001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0008-4001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f39b3e7d-39d2-4c8a-9974-4ab885241880