Skip to main content

Lisinopril and Hydrochlorothiazide

NDC 71205-763 · Proficient Rx LP

Generic nameLisinopril and Hydrochlorothiazide Tablets
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

71205-763-30 — 30 TABLET in 1 BOTTLE (71205-763-30)

71205-763-60 — 60 TABLET in 1 BOTTLE (71205-763-60)

71205-763-90 — 90 TABLET in 1 BOTTLE (71205-763-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-180 — Lisinopril, 71205-249 — Valsartan and Hydrochlorothiazide, 71205-258 — Valsartan and Hydrochlorothiazide, 71205-327 — Valsartan and Hydrochlorothiazide, 71205-419 — Hydrochlorothiazide, 71205-471 — Lisinopril, 71205-589 — Hydrochlorothiazide, 71205-626 — Lisinopril, 71205-742 — Lisinopril, 71205-751 — Hydrochlorothiazide, 71205-793 — hydrochlorothiazide, 71205-980 — Hydrochlorothiazide, 71335-0015 — Lisinopril, 71335-0067 — hydrochlorothiazide, 71335-0075 — Lisinopril, 71335-0145 — Hydrochlorothiazide, 71335-0152 — Losartan Potassium and Hydrochlorothiazide, 71335-0176 — Lisinopril, 71335-0269 — Hydrochlorothiazide, 71335-0326 — Triamterene and 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.