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AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE

NDC 72189-260 · DIRECT RX

Generic nameAMLODIPINE AND BENAZEPRIL HYDROCHLORIDE
Dosage formCAPSULE
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Strength10; 20 mg/1; mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Marketing categoryANDA

Packages

72189-260-90 — 90 CAPSULE in 1 BOTTLE (72189-260-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-2090 — Amlodipine and Atorvastatin, 72162-2091 — Amlodipine and Atorvastatin, 72162-2092 — Amlodipine and Atorvastatin, 72162-2093 — Amlodipine and Atorvastatin, 72162-2094 — Amlodipine and Atorvastatin, 72162-2328 — benazepril hydrochloride and hydrochlorothiazide, 72162-2360 — Amlodipine and Benazepril Hydrochloride, 72162-2379 — Amlodipine and Olmesartan Medoxomil, 72189-110 — BENAZEPRIL HYDROCHLORIDE, 72189-162 — AMLODIPINE BESYLATE, 72189-520 — Amlodipine Besylate, 72189-529 — Amlodipine Besylate, 72789-260 — AMLODIPINE BESYLATE, 72789-261 — AMLODIPINE BESYLATE, 72789-262 — AMLODIPINE BESYLATE, 72789-285 — Amlodipine and Benazepril Hydrochloride, 72789-412 — Amlodipine and Benazepril Hydrochloride, 72789-432 — Amlodipine Besylate and Benazepril Hydrochloride, 72789-502 — Amlodipine Besylate and Benazepril Hydrochloride, 72789-514 — Amlodipine Besylate, +624 more

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