Lisinopril and Hydrochlorothiazide

NDC 0591-0861 · Actavis Pharma, Inc.

Generic nameLisinopril and Hydrochlorothiazide

Dosage formTABLET

RouteORAL

Active ingredient(s)LISINOPRIL, HYDROCHLOROTHIAZIDE

Strength12.5; 20 mg/1; mg/1

Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Marketing categoryANDA

Packages

0591-0861-01 — 100 TABLET in 1 BOTTLE, PLASTIC (0591-0861-01)

0591-0861-05 — 500 TABLET in 1 BOTTLE, PLASTIC (0591-0861-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0574-0229 — benazepril hydrochloride and hydrochlorothiazide, 0591-0347 — Hydrochlorothiazide, 0591-0348 — Triamterene and Hydrochlorothiazide, 0591-0405 — Lisinopril, 0591-0406 — Lisinopril, 0591-0407 — Lisinopril, 0591-0408 — Lisinopril, 0591-0409 — Lisinopril, 0591-0424 — Triamterene and Hydrochlorothiazide, 0591-0860 — Lisinopril and Hydrochlorothiazide, 0591-0862 — Lisinopril and Hydrochlorothiazide, 0591-0885 — Lisinopril, 0597-0042 — telmisartan and hydrochlorothiazide, 0597-0043 — telmisartan and hydrochlorothiazide, 0597-0044 — telmisartan and hydrochlorothiazide, 0615-8252 — Lisinopril, 0615-8253 — Lisinopril, 0615-8254 — Lisinopril, 0615-8255 — Lisinopril, 0615-8344 — Hydrochlorothiazide, +1122 more

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