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
68180-765_e0777a79-35ef-4f69-b6ac-94d31f7ca6fb
Product NDC
68180-765
Form
TABLET
Composition / generic term
Amlodipine and Valsartan
Labeler
Lupin Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20150331
Source listing expiry
20261231

Source-listed ingredients

  • AMLODIPINE BESYLATE — 10 mg/1
  • VALSARTAN — 160 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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