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
- 71335-9609_d1a8c9e3-3ac2-476e-8a48-e117af47837d
- Product NDC
- 71335-9609
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-0) · 71335-9609-0
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-1) · 71335-9609-1
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-2) · 71335-9609-2
- 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-3) · 71335-9609-3
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-4) · 71335-9609-4
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-5) · 71335-9609-5
- 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-6) · 71335-9609-6
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-7) · 71335-9609-7
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-8) · 71335-9609-8
- 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-9) · 71335-9609-9
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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