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Amlodipine and Benazepril Hydrochloride

NDC 84677-013 · Golden State Medical Supply, Inc.

Generic nameAmlodipine 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

84677-013-01 — 100 CAPSULE in 1 BOTTLE (84677-013-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

81279-134 — amlodipine, 81279-135 — amlodipine, 82009-026 — AMLODIPINE BESYLATE, 82009-027 — AMLODIPINE BESYLATE, 82009-028 — AMLODIPINE BESYLATE, 82804-164 — Amlodipine Besylate, 82804-297 — Amlodipine besylate, 82804-969 — AMLODIPINE BESYLATE, 82804-970 — AMLODIPINE BESYLATE, 82804-971 — AMLODIPINE BESYLATE, 82868-031 — Amlodipine Besylate, 82868-041 — Amlodipine Besylate and Benazepril Hydrochloride, 82868-089 — Benazepril Hydrochloride, 83008-035 — Amlodipine Besylate, 83209-399 — Amlodipine Besylate, 84386-100 — Benazepril Hydrochloride, 84386-101 — Benazepril Hydrochloride, 84386-102 — Benazepril Hydrochloride, 87441-016 — Amlodipine besylate, 87441-017 — 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.