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
- 55111-645_8ebe8fd4-472a-4fb0-3a62-4bb87eb0381d
- Product NDC
- 55111-645
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140301
- Source listing expiry
- 20271231
Source-listed ingredients
- OMEPRAZOLE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-01) · 55111-645-01
- 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-05) · 55111-645-05
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-10) · 55111-645-10
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-645-30) · 55111-645-30
- 12 BOTTLE in 1 CARTON (55111-645-34) / 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-645-34
- 10 BLISTER PACK in 1 CARTON (55111-645-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-645-79) · 55111-645-78
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 →