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
84677-057_574d2577-f1ed-f6c4-e063-6394a90a0d4d
Product NDC
84677-057
Form
TABLET, FILM COATED
Composition / generic term
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Labeler
Golden State Medical Supply, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260331
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

  • 1000 TABLET, FILM COATED in 1 BOTTLE (84677-057-10) · 84677-057-10
  • 90 TABLET, FILM COATED in 1 BOTTLE (84677-057-90) · 84677-057-90

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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