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
- 76420-878_2dfff480-dff9-b242-e063-6394a90a1fcf
- Product NDC
- 76420-878
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141031
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-00) · 76420-878-00
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-01) · 76420-878-01
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-03) · 76420-878-03
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-06) · 76420-878-06
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-09) · 76420-878-09
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-12) · 76420-878-12
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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