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
- 71335-0299_b0b2453e-a5f6-4ad9-a113-720f562d0c7b
- Product NDC
- 71335-0299
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141031
- 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 (71335-0299-1) · 71335-0299-1
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-2) · 71335-0299-2
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-3) · 71335-0299-3
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-4) · 71335-0299-4
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-5) · 71335-0299-5
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-6) · 71335-0299-6
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-7) · 71335-0299-7
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-8) · 71335-0299-8
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →