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
- 50090-7018_b30a1877-ae69-4694-8cd7-cc1f910136fa
- Product NDC
- 50090-7018
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121123
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-0) · 50090-7018-0
- 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-2) · 50090-7018-2
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-3) · 50090-7018-3
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-4) · 50090-7018-4
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-5) · 50090-7018-5
- 200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-6) · 50090-7018-6
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-7) · 50090-7018-7
- 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7018-8) · 50090-7018-8
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 →