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Benazepril Hydrochloride

NDC 71335-0854 · Bryant Ranch Prepack

Generic nameBenazepril Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

71335-0854-1 — 30 TABLET in 1 BOTTLE (71335-0854-1)

71335-0854-2 — 60 TABLET in 1 BOTTLE (71335-0854-2)

71335-0854-3 — 100 TABLET in 1 BOTTLE (71335-0854-3)

71335-0854-4 — 90 TABLET in 1 BOTTLE (71335-0854-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4386 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4388 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4499 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4633 — Benazepril Hydrochloride, 71205-122 — Amlodipine and Benazepril Hydrochloride, 71205-244 — Benazepril Hydrochloride, 71205-320 — Benazepril Hydrochloride, 71335-0078 — Benazepril Hydrochloride, 71335-0267 — Benazepril Hydrochloride, 71335-0457 — Benazepril Hydrochloride, 71335-0953 — Amlodipine and Benazepril Hydrochloride, 71335-1086 — Benazepril Hydrochloride, 71335-1365 — Benazepril Hydrochloride, 71335-1946 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-2634 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3055 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3067 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3095 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3125 — Amlodipine Besylate and Benazepril Hydrochloride, 72162-1816 — 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.