Skip to main content

Amlodipine Besylate and Benazepril Hydrochloride

NDC 68001-133 · BluePoint Laboratories

Generic nameAmlodipine Besylate and Benazepril Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Strength5; 10 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

68001-133-00 — 100 CAPSULE in 1 BOTTLE (68001-133-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67877-499 — Amlodipine and olmesartan Medoxomil, 67877-500 — Amlodipine and olmesartan Medoxomil, 67877-501 — Amlodipine and olmesartan Medoxomil, 67877-502 — Amlodipine and olmesartan Medoxomil, 67877-900 — Amlodipine besylate, 67877-901 — Amlodipine besylate, 67877-902 — Amlodipine besylate, 68001-130 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-131 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-132 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-134 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-135 — Amlodipine Besylate and Benazepril Hydrochloride, 68071-1769 — Benazepril Hydrochloride, 68071-1770 — Benazepril Hydrochloride, 68071-1969 — Benazepril Hydrochloride, 68071-1980 — AMLODIPINE BESYLATE, 68071-2305 — Amlodipine Besylate, 68071-2520 — Amlodipine besylate, 68071-3057 — Benazepril Hydrochloride, 68071-3324 — 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.