# Pantoprazole Sodium

NDC: 31722-032
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GRANULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20231027

FDA application: ANDA216139

## 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:"31722-032"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-032
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee6278c0-d8c0-417c-a65c-b522ff76fe44