United States · FDA National Drug Code directory

olmesartan medoxomil-hydrochlorothiazide

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
73190-080_569596ad-cf4a-80be-e063-6394a90aa2aa
Product NDC
73190-080
Form
TABLET, FILM COATED
Composition / generic term
olmesartan medoxomil-hydrochlorothiazide
Labeler
AvKARE
Marketing category
NDA
Marketing start / end (source format)
20260714
Source listing expiry
20271231

Source-listed ingredients

  • OLMESARTAN MEDOXOMIL — 40 mg/1
  • HYDROCHLOROTHIAZIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED in 1 BOTTLE (73190-080-90) · 73190-080-90

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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