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
- 23155-921_ecbe2177-2319-4e49-a47a-48dd1aefe99f
- Product NDC
- 23155-921
- Form
- CAPSULE
- Composition / generic term
- Amlodipine and Benazepril Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260523
- Source listing expiry
- 20271231
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 (23155-921-01) · 23155-921-01
- 500 CAPSULE in 1 BOTTLE (23155-921-05) · 23155-921-05
- 1000 CAPSULE in 1 BOTTLE (23155-921-10) · 23155-921-10
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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