# Pantoprazole Sodium

NDC: 13668-096
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
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: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13668-096"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-096
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c983da1-a8e0-479e-8816-5d5668ea242e