# Pantoprazole Sodium

NDC: 42799-952
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GRANULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230616

FDA application: ANDA216247

## 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:"42799-952"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-952
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0bb76bc-094a-4d61-9bb2-2226c9da4ae9