United States · FDA National Drug Code directory

Omeprazole Magnesium

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
69842-027_337e6afa-c24a-94b7-5b3f-2a8d477ac2a9
Product NDC
69842-027
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Omeprazole Magnesium
Labeler
CVS Health Corp.
Marketing category
ANDA
Marketing start / end (source format)
20111101
Source listing expiry
20261231

Source-listed ingredients

  • OMEPRAZOLE MAGNESIUM — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BOTTLE in 1 CARTON (69842-027-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 69842-027-01
  • 1 BOTTLE in 1 CARTON (69842-027-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 69842-027-14
  • 2 BOTTLE in 1 CARTON (69842-027-28) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 69842-027-28
  • 3 BOTTLE in 1 CARTON (69842-027-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 69842-027-42

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 →