United States · FDA National Drug Code directory
Pantoprazole sodium
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70095-024_b423abbc-01e1-4d07-9c89-a7398c898d2f
- Product NDC
- 70095-024
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Pantoprazole sodium
- Labeler
- Sun Pharmaceutical Industries Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230403
- Source listing expiry
- 20261231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CARTON in 1 PACKAGE (70095-024-02) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) · 70095-024-02
- 25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) · 70095-024-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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