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
- 60505-0146_8619e520-d106-4778-e92a-09b919b55c70
- Product NDC
- 60505-0146
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Apotex Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090121 / 20270131
Source-listed ingredients
- OMEPRAZOLE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-1) · 60505-0146-1
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-2) · 60505-0146-2
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 →