United States · FDA National Drug Code directory

Equate omeprazole delayed release acid reducer

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
49035-915_03d865a0-ac92-49d5-82e2-2276292add17
Product NDC
49035-915
Form
TABLET, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
Wal-Mart Stores Inc
Marketing category
NDA
Marketing start / end (source format)
20080227
Source listing expiry
20261231

Source-listed ingredients

  • OMEPRAZOLE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (49035-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 49035-915-01
  • 3 BOTTLE in 1 CARTON (49035-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 49035-915-03
  • 2 CARTON in 1 CARTON (49035-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 49035-915-30

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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