# pantoprazole sodium

NDC: 31722-204
Generic name: pantoprazole sodium
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220518

FDA application: ANDA213778

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1bb94d3c-8bc3-4193-9dd8-e9a22066707c