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Benazepril Hydrochloride

NDC 62559-527 · ANI Pharmaceuticals, Inc.

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

Packages

62559-527-01 — 100 TABLET in 1 BOTTLE (62559-527-01)

62559-527-05 — 500 TABLET in 1 BOTTLE (62559-527-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62559-524 — Benazepril Hydrochloride, 62559-525 — Benazepril Hydrochloride, 62559-526 — Benazepril Hydrochloride

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.