United States · FDA National Drug Code directory
Omeprazole Magnesium
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
- 55111-397_fff9af9d-87b4-7d54-4cc4-c65b07556ec5
- Product NDC
- 55111-397
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole Magnesium
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100301
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (55111-397-27) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-397-27
- 2 CARTON in 1 CARTON (55111-397-28) / 2 BLISTER PACK in 1 CARTON (55111-397-74) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 55111-397-28
- 3 BOTTLE in 1 CARTON (55111-397-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-397-33
- 3 BOTTLE in 1 CARTON (55111-397-39) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-397-39
- 3 CARTON in 1 CARTON (55111-397-42) / 2 BLISTER PACK in 1 CARTON (55111-397-74) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 55111-397-42
- 1 BOTTLE in 1 CARTON (55111-397-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-397-52
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 →