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
71335-0569_f5868802-1b1f-4d48-8793-39d25a65b0d8
Product NDC
71335-0569
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Omeprazole
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20031111 / 20270131

Source-listed ingredients

  • OMEPRAZOLE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-0) · 71335-0569-0
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-1) · 71335-0569-1
  • 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-2) · 71335-0569-2
  • 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-3) · 71335-0569-3
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-4) · 71335-0569-4
  • 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-5) · 71335-0569-5
  • 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-6) · 71335-0569-6
  • 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-7) · 71335-0569-7
  • 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-8) · 71335-0569-8
  • 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-9) · 71335-0569-9

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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