United States · FDA National Drug Code directory

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
53746-847_1ed15f09-2051-401f-a320-5f04b85ac8e2
Product NDC
53746-847
Form
TABLET, FILM COATED
Composition / generic term
Valsartan and Hydrochlorothiazide
Labeler
Amneal Pharmaceuticals of New York LLC
Marketing category
ANDA
Marketing start / end (source format)
20230814
Source listing expiry
20261231

Source-listed ingredients

  • VALSARTAN — 160 mg/1
  • HYDROCHLOROTHIAZIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED in 1 BOTTLE (53746-847-90) · 53746-847-90

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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