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
- 57237-161_aec12e35-60fb-416c-a2d0-a87cfdcb30a6
- Product NDC
- 57237-161
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150819
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-01) · 57237-161-01
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-30) · 57237-161-30
- 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-50) · 57237-161-50
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-90) · 57237-161-90
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99) · 57237-161-99
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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