United States · FDA National Drug Code directory

Omeprazole DR

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
80425-0169_4cf007cf-ee50-ce69-e063-6394a90a971a
Product NDC
80425-0169
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20141031
Source listing expiry
20271231

Source-listed ingredients

  • OMEPRAZOLE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0169-1) · 80425-0169-1
  • 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0169-2) · 80425-0169-2
  • 4 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0169-3) · 80425-0169-3

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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Omeprazole DR — United States | Molindra Medicines