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Benazepril Hydrochloride

NDC 43063-748 · PD-Rx Pharmaceuticals, Inc.

Generic nameBenazepril Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

43063-748-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-748-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-925 — Amlodipine and Benazepril Hydrochloride, 30698-448 — benazepril hydrochloride, 30698-449 — benazepril hydrochloride, 30698-450 — benazepril hydrochloride, 30698-452 — benazepril hydrochloride and hydrochlorothiazide, 30698-453 — benazepril hydrochloride and hydrochlorothiazide, 30698-454 — benazepril hydrochloride and hydrochlorothiazide, 42291-015 — Amlodipine and Benazepril Hydrochloride, 43063-677 — Benazepril Hydrochloride, 43063-679 — Benazepril Hydrochloride, 43547-335 — Benazepril Hydrochloride, 43547-336 — Benazepril Hydrochloride, 43547-337 — Benazepril Hydrochloride, 43547-338 — Benazepril Hydrochloride, 50090-0914 — Benazepril Hydrochloride, 50090-1042 — Amlodipine and Benazepril Hydrochloride, 50090-1418 — Amlodipine and Benazepril Hydrochloride, 50090-2720 — Amlodipine and Benazepril Hydrochloride, 50090-3243 — Benazepril Hydrochloride, 50090-3357 — 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.