United States · FDA National Drug Code directory

amlodipine,valsartan 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: 33342-284_1ea4f227-b97a-49f1-bbc3-1dede2c1866d
Product NDC: 33342-284
Form: TABLET, FILM COATED
Composition / generic term: amlodipine,valsartan and hydrochlorothiazide
Labeler: Macleods Pharmaceuticals Limited
Marketing category: ANDA
Marketing start / end (source format): 20250106
Source listing expiry: 20261231

Source-listed ingredients

AMLODIPINE BESYLATE — 10 mg/1
VALSARTAN — 160 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 (33342-284-07) · 33342-284-07
90 TABLET, FILM COATED in 1 BOTTLE (33342-284-10) · 33342-284-10
10 BLISTER PACK in 1 CARTON (33342-284-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 33342-284-12

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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