United States · FDA National Drug Code directory
omeprazole
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
- 45802-888_390ed372-f284-46b1-92bd-c2432fe6920b
- Product NDC
- 45802-888
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Marketing category
- NDA
- Marketing start / end (source format)
- 20080225
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 CARTON in 1 CARTON (45802-888-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 45802-888-30
- 3 CARTON in 1 CARTON (45802-888-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 45802-888-55
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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