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
- 65862-739_909d72a6-7116-407e-8ec8-77b9b5798237
- Product NDC
- 65862-739
- Form
- TABLET, FILM COATED
- Composition / generic term
- Amlodipine and valsartan
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160422
- 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
- 3 BLISTER PACK in 1 CARTON (65862-739-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-739-10) · 65862-739-03
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-739-30) · 65862-739-30
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-739-90) · 65862-739-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →