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
- 71335-1532_2d8d7573-8196-4fb8-bd73-351c763c5fd2
- Product NDC
- 71335-1532
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- omeprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090123
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-1) · 71335-1532-1
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-2) · 71335-1532-2
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-3) · 71335-1532-3
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-4) · 71335-1532-4
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-5) · 71335-1532-5
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-6) · 71335-1532-6
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-7) · 71335-1532-7
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-8) · 71335-1532-8
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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