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: 59640-699_b7d30cef-eb7f-482d-91c9-992c36525091
Product NDC: 59640-699
Form: CAPSULE, DELAYED RELEASE
Composition / generic term: Omeprazole
Labeler: H E B
Marketing category: ANDA
Marketing start / end (source format): 20260807
Source listing expiry: 20271231

Source-listed ingredients

OMEPRAZOLE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (59640-699-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59640-699-14) · 59640-699-01
3 BOTTLE in 1 CARTON (59640-699-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59640-699-14) · 59640-699-03

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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