# Pantoprazole

NDC: 55111-333
Generic name: Pantoprazole
Labeler / Manufacturer: Dr.Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20110119

FDA application: ANDA077619

## 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:"55111-333"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-333
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=564709e8-358f-c185-4ecb-b3849c3fe59c