United States · FDA National Drug Code directory
Prilosec OTC
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
- 37000-459_401e2c9f-fcc4-3d54-e063-6394a90a44e4
- Product NDC
- 37000-459
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- OMEPRAZOLE MAGNESIUM
- Labeler
- The Procter & Gamble Manufacturing Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 20120815
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET, DELAYED RELEASE in 1 POUCH (37000-459-01) · 37000-459-01
- 14 BLISTER PACK in 1 CARTON (37000-459-02) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 37000-459-02
- 3 CARTON in 1 CARTON (37000-459-04) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 37000-459-04
- 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (37000-459-05) · 37000-459-05
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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