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Benazepril Hydrochloride

NDC 68788-6957 · Preferred 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

68788-6957-1 — 100 TABLET, COATED in 1 BOTTLE (68788-6957-1)

68788-6957-3 — 30 TABLET, COATED in 1 BOTTLE (68788-6957-3)

68788-6957-6 — 60 TABLET, COATED in 1 BOTTLE (68788-6957-6)

68788-6957-8 — 120 TABLET, COATED in 1 BOTTLE (68788-6957-8)

68788-6957-9 — 90 TABLET, COATED in 1 BOTTLE (68788-6957-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-756 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-757 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-758 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-759 — Amlodipine Besylate and Benazepril Hydrochloride, 68180-760 — Amlodipine Besylate and Benazepril Hydrochloride, 68462-576 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-577 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-578 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-579 — Benazepril Hydrochloride and Hydrochlorothiazide, 68788-6889 — Benazepril Hydrochloride, 68788-8454 — Amlodipine and Benazepril Hydrochloride, 68788-8818 — Amlodipine Besylate and Benazepril Hydrochloride, 68788-8877 — Benazepril Hydrochloride, 68788-9313 — Benazepril Hydrochloride, 68788-9327 — Benazepril Hydrochloride, 69238-2684 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2685 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2686 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2687 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-1928 — 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.