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
- 30142-992_759b705a-526e-47e2-97f9-a78ab21a2c5d
- Product NDC
- 30142-992
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- omeprazole
- Labeler
- THE KROGER COMPANY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200715
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (30142-992-14) · 30142-992-14
- 2 TABLET, DELAYED RELEASE in 1 CARTON (30142-992-28) · 30142-992-28
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 →