# PANTOPRAZOLE SODIUM

NDC: 82009-010
Generic name: PANTOPRAZOLE
Labeler / Manufacturer: Quallent Pharmaceuticals Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220606

FDA application: ANDA202882

## Active ingredients

- PANTOPRAZOLE SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82009-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=643eb498-d916-4fb7-9281-32895575ab36