# Pantoprazole sodium delayed-release

NDC: 70756-019
Generic name: Pantoprazole sodium delayed-release
Labeler / Manufacturer: Lifestar Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220727

FDA application: ANDA215880

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70756-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70756-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0502f935-af7a-4f1e-8c3e-29e20647c885