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
- 83209-150_1ab3d2c4-43c7-504d-e063-6394a90a9ba9
- Product NDC
- 83209-150
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Omeprazole
- Labeler
- Boswell Pharmacy Services LLC d/b/a BPS Wholesale
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240612
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-05) · 83209-150-05
- 6 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-06) · 83209-150-06
- 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-10) · 83209-150-10
- 15 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-15) · 83209-150-15
- 20 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-20) · 83209-150-20
- 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (83209-150-30) · 83209-150-30
Source and coverage
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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.
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