Amlodipine and Benazepril Hydrochloride

NDC 50090-1042 · A-S Medication Solutions

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

50090-1042-0 — 30 CAPSULE in 1 BOTTLE (50090-1042-0)

50090-1042-1 — 90 CAPSULE in 1 BOTTLE (50090-1042-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-765 — Amlodipine and Atorvastatin, 48433-155 — Amlodipine Besylate, 48433-156 — Amlodipine Besylate, 48433-157 — Amlodipine Besylate, 49884-786 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-787 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-788 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-789 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-790 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 50090-0914 — Benazepril Hydrochloride, 50090-1418 — Amlodipine and Benazepril Hydrochloride, 50090-1627 — Amlodipine besylate, 50090-2524 — Amlodipine besylate, 50090-2581 — Amlodipine besylate, 50090-2720 — Amlodipine and Benazepril Hydrochloride, 50090-3243 — Benazepril Hydrochloride, 50090-3357 — Amlodipine and Benazepril Hydrochloride, 50090-3359 — Benazepril Hydrochloride, 50090-3775 — Benazepril Hydrochloride, 50090-4284 — Amlodipine and Benazepril Hydrochloride, +624 more

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