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
- 55111-158_0dc50704-e0d5-1fcc-b0b5-6e5556db65e8
- Product NDC
- 55111-158
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090121
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-158-01) · 55111-158-01
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-158-10) · 55111-158-10
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-158-30) · 55111-158-30
- 12 BOTTLE in 1 CARTON (55111-158-34) / 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-158-34
- 10 BLISTER PACK in 1 CARTON (55111-158-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-158-79) · 55111-158-78
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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