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
- 65219-385_452b14d4-4fbd-47b1-b4b1-f0b302e8f0d9
- Product NDC
- 65219-385
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Pantoprazole Sodium
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240801
- Source listing expiry
- 20261231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (65219-385-10) / 10 mL in 1 VIAL (65219-385-01) · 65219-385-10
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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