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
- 71335-1851_ef9510bf-050b-44e7-a6bc-5b913f9025ce
- Product NDC
- 71335-1851
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150819
- 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 (71335-1851-1) · 71335-1851-1
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-2) · 71335-1851-2
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-3) · 71335-1851-3
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-4) · 71335-1851-4
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-5) · 71335-1851-5
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-6) · 71335-1851-6
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-7) · 71335-1851-7
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-8) · 71335-1851-8
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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