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
31722-888_3d401487-0f8f-9ee8-e063-6394a90ac68d
Product NDC
31722-888
Form
TABLET, FILM COATED
Composition / generic term
Olmesartan medoxomil and hydrochlorothiazide
Labeler
Camber Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250725
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 (31722-888-30) · 31722-888-30
  • 10 BLISTER PACK in 1 CARTON (31722-888-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 31722-888-32
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90) · 31722-888-90

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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