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Benazepril Hydrochloride

NDC 65162-754 · Amneal Pharmaceuticals LLC

Generic nameBenazepril Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

65162-754-03 — 30 TABLET in 1 BOTTLE (65162-754-03)

65162-754-10 — 100 TABLET in 1 BOTTLE (65162-754-10)

65162-754-50 — 500 TABLET in 1 BOTTLE (65162-754-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62559-416 — Benazepril Hydrochloride and Hydrochlorothiazide, 62559-417 — Benazepril Hydrochloride and Hydrochlorothiazide, 63187-393 — Benazepril Hydrochloride, 63187-499 — Benazepril Hydrochloride, 63187-500 — Benazepril Hydrochloride, 63187-906 — Benazepril Hydrochloride, 63629-7535 — Amlodipine and Benazepril Hydrochloride, 65162-751 — Benazepril Hydrochloride, 65162-752 — Benazepril Hydrochloride, 65162-753 — Benazepril Hydrochloride, 65862-117 — Benazepril Hydrochloride, 65862-118 — Benazepril Hydrochloride, 65862-582 — Amlodipine and Benazepril Hydrochloride, 65862-583 — Amlodipine and Benazepril Hydrochloride, 65862-584 — Amlodipine and Benazepril Hydrochloride, 65862-585 — Amlodipine and Benazepril Hydrochloride, 65862-586 — Amlodipine and Benazepril Hydrochloride, 65862-587 — Amlodipine and Benazepril Hydrochloride, 68001-130 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-131 — Amlodipine Besylate and 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.