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Amlodipine Besylate and Benazepril Hydrochloride

NDC 70518-4382 · REMEDYREPACK INC.

Generic nameAmlodipine Besylate and Benazepril Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Strength10; 40 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

70518-4382-0 — 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4382-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-0297 — AMLODIPINE BESYLATE, 70518-0835 — AMLODIPINE BESYLATE, 70518-1928 — Amlodipine and Benazepril Hydrochloride, 70518-1971 — Amlodipine besylate, 70518-2125 — Benazepril Hydrochloride, 70518-2566 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-2632 — Amlodipine besylate, 70518-2981 — Amlodipine besylate, 70518-3592 — Amlodipine Besylate, 70518-4165 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 70518-4386 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4388 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4464 — Amlodipine Besylate, 70518-4499 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4629 — Amlodipine besylate, 70518-4633 — Benazepril Hydrochloride, 71205-122 — Amlodipine and Benazepril Hydrochloride, 71205-244 — Benazepril Hydrochloride, 71205-320 — Benazepril Hydrochloride, 71205-488 — 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.