United States · FDA National Drug Code directory
Omeprazole Delayed release
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
- 61269-720_35eb1fd8-d750-499e-8bef-cbdcb23aab7b
- Product NDC
- 61269-720
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- H2-Pharma, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260804
- Source listing expiry
- 20271231
Source-listed ingredients
- OMEPRAZOLE MAGNESIUM — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (61269-720-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 61269-720-14
- 3 BOTTLE in 1 CARTON (61269-720-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 61269-720-42
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 →