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
- 0781-2859_b182f298-e28f-434b-b6f1-ecfac29d495e
- Product NDC
- 0781-2859
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20271231
Source-listed ingredients
- OMEPRAZOLE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-01) · 0781-2859-01
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-10) · 0781-2859-10
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-31) · 0781-2859-31
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-92) · 0781-2859-92
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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