United States · FDA National Drug Code directory
signature care 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
- 21130-401_fd87b124-5abc-4db7-9125-350ac1699a1d
- Product NDC
- 21130-401
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- omeprazole
- Labeler
- Safeway
- Marketing category
- NDA
- Marketing start / end (source format)
- 20200811
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (21130-401-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 21130-401-01
- 3 BOTTLE in 1 CARTON (21130-401-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 21130-401-03
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 →