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
- 37000-455_401e1256-05e3-d4a9-e063-6294a90adce4
- Product NDC
- 37000-455
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- omeprazole magnesium
- Labeler
- The Procter & Gamble Manufacturing Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 20030714
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 20.6 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET, DELAYED RELEASE in 1 POUCH (37000-455-01) · 37000-455-01
- 1 BLISTER PACK in 1 CARTON (37000-455-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 37000-455-02
- 2 CARTON in 1 CARTON (37000-455-03) / 1 BLISTER PACK in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 37000-455-03
- 3 CARTON in 1 CARTON (37000-455-04) / 1 BLISTER PACK in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 37000-455-04
- 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (37000-455-05) · 37000-455-05
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →