# Pantoprazole Sodium

NDC: 55150-202
Generic name: Pantoprazole Sodium
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20160330

FDA application: ANDA205675

## 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:"55150-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9bed093a-9586-4c82-a2b7-c68f89d0faef