United States · FDA National Drug Code directory

Olmesartan medoxomil

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
33342-179_0e3686f3-0150-49d0-b359-dcd05fa98fd7
Product NDC
33342-179
Form
TABLET
Composition / generic term
Olmesartan medoxomil
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20170425
Source listing expiry
20271231

Source-listed ingredients

  • OLMESARTAN MEDOXOMIL — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (33342-179-07) · 33342-179-07
  • 90 TABLET in 1 BOTTLE (33342-179-10) · 33342-179-10
  • 10 BLISTER PACK in 1 CARTON (33342-179-12) / 10 TABLET in 1 BLISTER PACK · 33342-179-12
  • 1000 TABLET in 1 BOTTLE (33342-179-44) · 33342-179-44

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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