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: 68180-774_5e938b33-b86d-40ab-b5c5-b7137ef9404d
Product NDC: 68180-774
Form: TABLET, FILM COATED
Composition / generic term: Amlodipine, Valsartan and Hydrochlorothiazide
Labeler: Lupin Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20150604
Source listing expiry: 20261231

Source-listed ingredients

AMLODIPINE BESYLATE — 10 mg/1
VALSARTAN — 160 mg/1
HYDROCHLOROTHIAZIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

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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