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Lisinopril and Hydrochlorothiazide

NDC 68071-4435 · NuCare Pharmaceuticals,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

68071-4435-3 — 30 TABLET in 1 BOTTLE (68071-4435-3)

68071-4435-6 — 60 TABLET in 1 BOTTLE (68071-4435-6)

68071-4435-9 — 90 TABLET in 1 BOTTLE (68071-4435-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3178 — Lisinopril, 68071-3220 — Lisinopril, 68071-3323 — Hydrochlorothiazide, 68071-3409 — Lisinopril, 68071-3411 — Lisinopril, 68071-3443 — Hydrochlorothiazide, 68071-3608 — HYDROCHLOROTHIAZIDE, 68071-3652 — HYDROCHLOROTHIAZIDE, 68071-3879 — Triamterene and Hydrochlorothiazide, 68071-4159 — Losartan Potassium and Hydrochlorothiazide, 68071-4518 — Losartan Potassium and Hydrochlorothiazide, 68071-4660 — Lisinopril, 68071-4687 — Triamterene and Hydrochlorothiazide, 68071-4819 — Hydrochlorothiazide, 68071-4858 — Lisinopril, 68071-4933 — Hydrochlorothiazide, 68071-4963 — Hydrochlorothiazide, 68071-5036 — Lisinopril, 68071-5046 — Lisinopril, 68071-5089 — Lisinopril, +1122 more

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