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Lotensin

NDC 30698-448 · Validus Pharmaceuticals LLC

Generic namebenazepril hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)BENAZEPRIL HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryNDA

Packages

30698-448-01 — 100 TABLET in 1 BOTTLE (30698-448-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-749 — Benazepril Hydrochloride, 23155-750 — Benazepril Hydrochloride, 23155-751 — Benazepril Hydrochloride, 23155-752 — Benazepril Hydrochloride, 23155-920 — Amlodipine and Benazepril Hydrochloride, 23155-921 — Amlodipine and Benazepril Hydrochloride, 23155-922 — Amlodipine and Benazepril Hydrochloride, 23155-923 — Amlodipine and Benazepril Hydrochloride, 23155-924 — Amlodipine and Benazepril Hydrochloride, 23155-925 — Amlodipine and 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, 43063-748 — Benazepril Hydrochloride, 43547-335 — 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.