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
55154-2332_b791235a-9992-434e-9b31-bbd5ed4e1c81
Product NDC
55154-2332
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
Cardinal Health 107, LLC
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

  • 10 BLISTER PACK in 1 BAG (55154-2332-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 55154-2332-0

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.

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