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
- 72205-149_c8197eea-e990-4c0e-bc2d-f080bac8de17
- Product NDC
- 72205-149
- Form
- TABLET, FILM COATED
- Composition / generic term
- olmesartan medoxomil-hydrochlorothiazide
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250926
- Source listing expiry
- 20261231
Source-listed ingredients
- OLMESARTAN MEDOXOMIL — 40 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (72205-149-30) · 72205-149-30
- 90 TABLET, FILM COATED in 1 BOTTLE (72205-149-90) · 72205-149-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (72205-149-99) · 72205-149-99
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →