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Benazepril Hydrochloride

NDC 51407-465 · Golden State Medical Supply, Inc.

Generic nameBenazepril Hydrochloride
Dosage formTABLET, COATED
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

51407-465-01 — 100 TABLET, COATED in 1 BOTTLE (51407-465-01)

51407-465-05 — 500 TABLET, COATED in 1 BOTTLE (51407-465-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6427 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-6770 — Amlodipine and Benazepril Hydrochloride, 50090-7361 — Amlodipine and Benazepril Hydrochloride, 50268-109 — Benazepril Hydrochloride, 50268-110 — Benazepril Hydrochloride, 50268-111 — Benazepril Hydrochloride, 50268-112 — Benazepril Hydrochloride, 51407-462 — Benazepril Hydrochloride, 51407-463 — Benazepril Hydrochloride, 51407-464 — Benazepril Hydrochloride, 51655-065 — Benazepril Hydrochloride, 51655-066 — Benazepril Hydrochloride, 51655-201 — Amlodipine Besylate and Benazepril Hydrochloride, 51655-202 — Benazepril Hydrochloride, 51655-213 — Amlodipine and Benazepril Hydrochloride, 51655-388 — Benazepril Hydrochloride, 51655-617 — Benazepril Hydrochloride, 51655-755 — Benazepril Hydrochloride, 53746-751 — Benazepril Hydrochloride, 53746-752 — 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.