# PANTOPRAZOLE SODIUM

NDC: 72189-112
Generic name: pantoprazole
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200612

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:"72189-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a7e7c1ab-3e75-1ff8-e053-2995a90a7539