# PANTOPRAZOLE SODIUM

NDC: 62332-071
Generic name: pantoprazole sodium injection
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250331

FDA application: ANDA219230

## Active ingredients

- PANTOPRAZOLE SODIUM: 40 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-071"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-071
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9e5fac6-2db6-4311-a98b-eb3f0dde19d6