United States · FDA National Drug Code directory
Olmesartan Medoxomil, Amlodipine and 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
- 0093-5004_a035edd9-948f-4168-b74b-9961a2cb219a
- Product NDC
- 0093-5004
- Form
- TABLET, FILM COATED
- Composition / generic term
- Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161114
- Source listing expiry
- 20261231
Source-listed ingredients
- OLMESARTAN MEDOXOMIL — 40 mg/1
- AMLODIPINE BESYLATE — 5 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (0093-5004-56) · 0093-5004-56
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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