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
- 63187-070_0cc267bf-8650-40e3-a05d-e102e275c4c2
- Product NDC
- 63187-070
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20031111 / 20270131
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-14) · 63187-070-14
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-30) · 63187-070-30
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-60) · 63187-070-60
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-72) · 63187-070-72
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-78) · 63187-070-78
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-90) · 63187-070-90
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 →