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Benazepril Hydrochloride

NDC 50268-111 · AvPAK

Generic nameBenazepril Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

50268-111-15 — 50 BLISTER PACK in 1 BOX (50268-111-15) / 1 TABLET in 1 BLISTER PACK (50268-111-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-5389 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5404 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-5750 — Benazepril Hydrochloride, 50090-5751 — Benazepril Hydrochloride, 50090-6185 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-6427 — Amlodipine Besylate and Benazepril Hydrochloride, 50090-6770 — Amlodipine and Benazepril Hydrochloride, 50090-7361 — Amlodipine and Benazepril Hydrochloride, 50268-109 — Benazepril Hydrochloride, 50268-110 — Benazepril Hydrochloride, 50268-112 — Benazepril Hydrochloride, 51407-462 — Benazepril Hydrochloride, 51407-463 — Benazepril Hydrochloride, 51407-464 — Benazepril Hydrochloride, 51407-465 — Benazepril Hydrochloride, 51655-065 — Benazepril Hydrochloride, 51655-066 — Benazepril Hydrochloride, 51655-201 — Amlodipine Besylate and Benazepril Hydrochloride, 51655-202 — Benazepril Hydrochloride, 51655-213 — Amlodipine and Benazepril Hydrochloride, +173 more

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