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
- 0078-1287_a2f8e96b-1cbc-4d5a-b61d-af5b990f1ece
- Product NDC
- 0078-1287
- Form
- TABLET, FILM COATED
- Composition / generic term
- amlodipine valsartan and hydrochlorothiazide
- Labeler
- Novartis Pharmaceuticals Corporation
- Marketing category
- DRUG FOR FURTHER PROCESSING
- Marketing start / end (source format)
- 20090404
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
- VALSARTAN — 160 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25000 TABLET, FILM COATED in 1 DRUM (0078-1287-01) · 0078-1287-01
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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