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Benazepril Hydrochloride

NDC 84386-101 · Aurobindo Pharma Limited

Generic nameBenazepril Hydrochloride
Dosage formTABLET, FILM 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

84386-101-01 — 100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01)

84386-101-90 — 90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 72162-2328 — benazepril hydrochloride and hydrochlorothiazide, 72162-2360 — Amlodipine and Benazepril Hydrochloride, 72189-110 — BENAZEPRIL HYDROCHLORIDE, 72189-260 — AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE, 72789-285 — Amlodipine and Benazepril Hydrochloride, 72789-412 — Amlodipine and Benazepril Hydrochloride, 72789-432 — Amlodipine Besylate and Benazepril Hydrochloride, 72789-502 — Amlodipine Besylate and Benazepril Hydrochloride, 72888-220 — benazepril hydrochloride and hydrochlorothiazide, 72888-221 — benazepril hydrochloride and hydrochlorothiazide, 72888-222 — benazepril hydrochloride and hydrochlorothiazide, 82868-041 — Amlodipine Besylate and Benazepril Hydrochloride, 82868-089 — Benazepril Hydrochloride, 84386-100 — Benazepril Hydrochloride, 84386-102 — Benazepril Hydrochloride, 84677-013 — Amlodipine 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.