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Lisinopril and Hydrochlorothiazide

NDC 68071-2183 · NuCare Pharmaceuticals,Inc.

Generic nameLisinopril and Hydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE, LISINOPRIL
Strength12.5; 10 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

68071-2183-9 — 90 TABLET in 1 BOTTLE (68071-2183-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-335 — Lisinopril, 68001-336 — Lisinopril, 68001-387 — Triamterene and Hydrochlorothiazide, 68001-388 — Triamterene and Hydrochlorothiazide, 68001-486 — Lisinopril, 68071-1672 — Lisinopril, 68071-1775 — Lisinopril, 68071-1834 — Triamterene and Hydrochlorothiazide, 68071-1894 — Lisinopril, 68071-1945 — Lisinopril and Hydrochlorothiazide, 68071-2224 — Lisinopril, 68071-2263 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2291 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2303 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2371 — Triamterene and Hydrochlorothiazide, 68071-2405 — Hydrochlorothiazide, 68071-2411 — Hydrochlorothiazide, 68071-2533 — Triamterene and Hydrochlorothiazide, 68071-2740 — Lisinopril and Hydrochlorothiazide Tablets, 68071-3008 — Lisinopril 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.