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
- 68180-775_5e938b33-b86d-40ab-b5c5-b7137ef9404d
- Product NDC
- 68180-775
- 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 — 320 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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