# Pantoprazole Sodium

NDC: 68071-1963
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20110120

FDA application: ANDA090074

## 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:"68071-1963"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-1963
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fbec80c-b38d-122c-e054-00144ff88e88