Quinapril

NDC 71205-635 · Proficient Rx LP

Generic nameQuinapril

Dosage formTABLET

RouteORAL

Active ingredient(s)QUINAPRIL HYDROCHLORIDE

Strength10 mg/1

Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

Marketing categoryANDA

Packages

71205-635-30 — 30 TABLET in 1 BOTTLE (71205-635-30)

71205-635-60 — 60 TABLET in 1 BOTTLE (71205-635-60)

71205-635-90 — 90 TABLET in 1 BOTTLE (71205-635-90)

FDA lists these products with the same active ingredient.

65862-619 — Quinapril Hydrochloride, 65862-620 — Quinapril Hydrochloride, 68001-187 — Quinapril, 68001-188 — Quinapril, 68001-189 — Quinapril, 68001-260 — Quinapril, 68180-554 — Quinapril, 68180-557 — Quinapril, 68180-558 — Quinapril, 68180-559 — Quinapril, 69097-828 — quinapril and Hydrochlorothiazide 10/12.5, 69097-829 — Quinapril and Hydrochlorothiazide 20/12.5, 69097-831 — Quinapril and Hydrochlorothiazide 20/25, 69097-839 — Quinapril, 69097-841 — Quinapril, 69097-842 — Quinapril, 69097-843 — Quinapril, 71205-484 — quinapril, 71335-1134 — quinapril, 71335-1707 — Quinapril, +24 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.