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Benazepril Hydrochloride

NDC 23155-751 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Generic nameBenazepril Hydrochloride
Dosage formTABLET
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

23155-751-01 — 100 TABLET in 1 BOTTLE (23155-751-01)

23155-751-05 — 500 TABLET in 1 BOTTLE (23155-751-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0078-0405 — amlodipine besylate and benazepril hydrochloride, 0078-0406 — amlodipine besylate and benazepril hydrochloride, 0185-0211 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0236 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0277 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0325 — Benazepril Hydrochloride and Hydrochlorothiazide, 0574-0228 — benazepril hydrochloride and hydrochlorothiazide, 0574-0229 — benazepril hydrochloride and hydrochlorothiazide, 23155-749 — Benazepril Hydrochloride, 23155-750 — Benazepril Hydrochloride, 23155-752 — Benazepril Hydrochloride, 23155-920 — Amlodipine and Benazepril Hydrochloride, 23155-921 — Amlodipine and Benazepril Hydrochloride, 23155-922 — Amlodipine and Benazepril Hydrochloride, 23155-923 — Amlodipine and Benazepril Hydrochloride, 23155-924 — Amlodipine and Benazepril Hydrochloride, 23155-925 — Amlodipine and Benazepril Hydrochloride, 30698-448 — benazepril hydrochloride, 30698-449 — benazepril hydrochloride, 30698-450 — 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.