United States · FDA National Drug Code directory
Protonix Delayed-Release
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
- 0008-0843_b1adaee5-9353-48ce-bde4-f169a3787e30
- Product NDC
- 0008-0843
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- PANTOPRAZOLE SODIUM
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20000501
- Source listing expiry
- 20271231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0843-81) · 0008-0843-81
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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