United States · FDA National Drug Code directory
up and up 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
- 11673-018_a8a64ea9-0d2c-45d5-a81d-da0d8ce60044
- Product NDC
- 11673-018
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Target Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 20150417
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (11673-018-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 11673-018-01
- 3 BOTTLE in 1 CARTON (11673-018-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 11673-018-03
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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