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Benazepril Hydrochloride

NDC 68071-1770 · NuCare Pharmaceuticals,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

68071-1770-1 — 100 TABLET, COATED in 1 BOTTLE (68071-1770-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-585 — Amlodipine and Benazepril Hydrochloride, 65862-586 — Amlodipine and Benazepril Hydrochloride, 65862-587 — Amlodipine and Benazepril Hydrochloride, 68001-130 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-131 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-132 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-133 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-134 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-135 — Amlodipine Besylate and Benazepril Hydrochloride, 68071-1769 — Benazepril Hydrochloride, 68071-1969 — Benazepril Hydrochloride, 68071-3057 — Benazepril Hydrochloride, 68071-3324 — Benazepril Hydrochloride, 68071-4722 — Benazepril Hydrochloride, 68071-5028 — Benazepril Hydrochloride, 68071-5129 — Benazepril Hydrochloride, 68071-5130 — Benazepril Hydrochloride, 68180-459 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-463 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-472 — Amlodipine Besylate 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.