United States · FDA National Drug Code directory

Omeprazole 20 mg

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: 25000-091_dcf79426-6aec-432a-aabe-dcb98c0f2cec
Product NDC: 25000-091
Form: TABLET, DELAYED RELEASE
Composition / generic term: Omeprazole 20 mg
Labeler: MARKSANS PHARMA LIMITED
Marketing category: ANDA
Marketing start / end (source format): 20250812
Source listing expiry: 20261231

Source-listed ingredients

OMEPRAZOLE MAGNESIUM — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (25000-091-76) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 25000-091-76
2 BLISTER PACK in 1 CARTON (25000-091-77) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 25000-091-77

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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