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Benazepril Hydrochloride

NDC 50090-3243 · A-S Medication Solutions

Generic nameBenazepril Hydrochloride
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

50090-3243-0 — 30 TABLET, COATED in 1 BOTTLE (50090-3243-0)

50090-3243-1 — 90 TABLET, COATED in 1 BOTTLE (50090-3243-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43063-679 — Benazepril Hydrochloride, 43063-748 — Benazepril Hydrochloride, 43547-335 — Benazepril Hydrochloride, 43547-336 — Benazepril Hydrochloride, 43547-337 — Benazepril Hydrochloride, 43547-338 — Benazepril Hydrochloride, 50090-0914 — Benazepril Hydrochloride, 50090-1042 — Amlodipine and Benazepril Hydrochloride, 50090-1418 — Amlodipine and Benazepril Hydrochloride, 50090-2720 — Amlodipine and Benazepril Hydrochloride, 50090-3357 — Amlodipine and Benazepril Hydrochloride, 50090-3359 — Benazepril Hydrochloride, 50090-3775 — Benazepril Hydrochloride, 50090-4284 — Amlodipine and Benazepril Hydrochloride, 50090-5137 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5357 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5389 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5404 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5750 — Benazepril Hydrochloride, 50090-5751 — Benazepril Hydrochloride, +173 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.