United States · FDA National Drug Code directory
Amlodipine and Benazepril Hydrochloride
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
- 65862-583_a45ec3e8-1d14-4c27-9685-976323df8cad
- Product NDC
- 65862-583
- Form
- CAPSULE
- Composition / generic term
- Amlodipine and Benazepril Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120905
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
- BENAZEPRIL HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (65862-583-01) · 65862-583-01
- 500 CAPSULE in 1 BOTTLE (65862-583-05) · 65862-583-05
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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