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Amlodipine and Benazepril Hydrochloride

NDC 65862-584 · Aurobindo Pharma Limited

Generic nameAmlodipine and Benazepril Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Strength5; 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

65862-584-01 — 100 CAPSULE in 1 BOTTLE (65862-584-01)

65862-584-05 — 500 CAPSULE in 1 BOTTLE (65862-584-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65841-620 — Amlodipine Besylate, 65841-621 — Amlodipine Besylate, 65841-622 — Amlodipine Besylate, 65862-101 — Amlodipine Besylate, 65862-102 — Amlodipine Besylate, 65862-103 — Amlodipine Besylate, 65862-117 — Benazepril Hydrochloride, 65862-118 — Benazepril Hydrochloride, 65862-582 — Amlodipine and Benazepril Hydrochloride, 65862-583 — Amlodipine and Benazepril Hydrochloride, 65862-585 — Amlodipine and Benazepril Hydrochloride, 65862-586 — Amlodipine and Benazepril Hydrochloride, 65862-587 — Amlodipine and Benazepril Hydrochloride, 65862-737 — Amlodipine and valsartan, 65862-738 — Amlodipine and valsartan, 65862-739 — Amlodipine and valsartan, 65862-740 — Amlodipine and valsartan, 65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, +624 more

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