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
70677-1098_252eeb77-6319-49df-9259-fcf2f917b2b5
Product NDC
70677-1098
Form
TABLET, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
STRATEGIC SOURCING SERVICES LLC
Marketing category
ANDA
Marketing start / end (source format)
20230811
Source listing expiry
20261231

Source-listed ingredients

  • OMEPRAZOLE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (70677-1098-1) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 70677-1098-1

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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