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
51407-943_3ba5e1e5-159d-2492-e063-6294a90a6c8b
Product NDC
51407-943
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
Golden State Medical Supply, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20241227
Source listing expiry
20261231

Source-listed ingredients

  • OMEPRAZOLE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 CAPSULE, DELAYED RELEASE in 1 PAIL (51407-943-00) · 51407-943-00
  • 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-943-01) · 51407-943-01
  • 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-943-05) · 51407-943-05
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-943-90) · 51407-943-90

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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