United States · FDA National Drug Code directory

Amlodipine and Valsartan

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: 23155-846_a1e93c2f-051c-40b9-a0ba-bfcf78a9c2d4
Product NDC: 23155-846
Form: TABLET
Composition / generic term: amlodipine and valsartan
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20230315
Source listing expiry: 20261231

Source-listed ingredients

AMLODIPINE — 5 mg/1
VALSARTAN — 320 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (23155-846-03) · 23155-846-03
90 TABLET in 1 BOTTLE, PLASTIC (23155-846-09) · 23155-846-09

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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