United States · FDA National Drug Code directory

candesartan cilexetil 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
43547-459_745438ab-c3fe-4da9-9548-730970399e0d
Product NDC
43547-459
Form
TABLET
Composition / generic term
candesartan cilexetil and hydrochlorothiazide
Labeler
Solco Healthcare LLC
Marketing category
ANDA
Marketing start / end (source format)
20171120
Source listing expiry
20261231

Source-listed ingredients

  • CANDESARTAN CILEXETIL — 16 mg/1
  • HYDROCHLOROTHIAZIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (43547-459-09) · 43547-459-09
  • 500 TABLET in 1 BOTTLE (43547-459-50) · 43547-459-50

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.

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candesartan cilexetil and hydrochlorothiazide — United States | Molindra Medicines