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
- 50090-7472_7159c642-41a8-41a4-b149-dc0d83b6c1ab
- Product NDC
- 50090-7472
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140301
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-0) · 50090-7472-0
- 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-2) · 50090-7472-2
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-3) · 50090-7472-3
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-4) · 50090-7472-4
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-5) · 50090-7472-5
- 200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-6) · 50090-7472-6
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-7) · 50090-7472-7
- 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-8) · 50090-7472-8
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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