United States · FDA National Drug Code directory

OLMESARTAN MEDOXOMIL 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: 67877-452_ffb1336b-75c4-483d-85d9-17b78237e915
Product NDC: 67877-452
Form: TABLET, FILM COATED
Composition / generic term: OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
Labeler: Ascend Laboratories, LLC
Marketing category: ANDA
Marketing start / end (source format): 20250501
Source listing expiry: 20271231

Source-listed ingredients

OLMESARTAN MEDOXOMIL — 40 mg/1
HYDROCHLOROTHIAZIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE (67877-452-30) · 67877-452-30
90 TABLET, FILM COATED in 1 BOTTLE (67877-452-90) · 67877-452-90

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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