United States · FDA National Drug Code directory

members mark 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: 68196-700_7292128d-5bd2-4239-b53d-22ec365a835e
Product NDC: 68196-700
Form: TABLET, DELAYED RELEASE
Composition / generic term: Omeprazole
Labeler: Sam's West Inc
Marketing category: NDA
Marketing start / end (source format): 20240207
Source listing expiry: 20261231

Source-listed ingredients

OMEPRAZOLE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

14 TABLET, DELAYED RELEASE in 1 BOTTLE (68196-700-01) · 68196-700-01
3 BOTTLE in 1 CARTON (68196-700-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 68196-700-03

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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