United States · FDA National Drug Code directory
Lotrel
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
- 0078-0364_b9db75d9-9d1e-4b2d-9876-5f5520feaecc
- Product NDC
- 0078-0364
- Form
- CAPSULE
- Composition / generic term
- amlodipine besylate and benazepril hydrochloride
- Labeler
- Novartis Pharmaceuticals Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 19950303 / 20260930
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
- BENAZEPRIL HYDROCHLORIDE — 20 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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