United States · FDA National Drug Code directory
Protonix I.V.
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
- 0008-0923_a7e7d657-a748-4234-8dd6-c0e4d0f81a86
- Product NDC
- 0008-0923
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- PANTOPRAZOLE SODIUM
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20010501
- Source listing expiry
- 20261231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (0008-0923-51) / 10 mL in 1 VIAL · 0008-0923-51
- 10 CARTON in 1 PACKAGE (0008-0923-55) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL · 0008-0923-55
- 25 CARTON in 1 PACKAGE (0008-0923-60) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL · 0008-0923-60
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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