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
- 0378-6689_38896560-f523-4d0b-8113-5ff7f5f38c81
- Product NDC
- 0378-6689
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- pantoprazole sodium
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110119
- Source listing expiry
- 20261231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-10) · 0378-6689-10
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-77) · 0378-6689-77
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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