United States · FDA National Drug Code directory
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
- 43547-335_fc8f15d2-3382-4933-a6bb-b1c57d50d57b
- Product NDC
- 43547-335
- Form
- TABLET, COATED
- Composition / generic term
- Benazepril Hydrochloride
- Labeler
- Solco healthcare U.S., LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140101
- Source listing expiry
- 20261231
Source-listed ingredients
- BENAZEPRIL HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (43547-335-03) · 43547-335-03
- 100 TABLET, COATED in 1 BOTTLE (43547-335-10) · 43547-335-10
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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