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LISINOPRIL

NDC 68071-3123 · NuCare Pharmaceuticals, Inc.

Generic nameLisinopril
Dosage formTABLET
RouteORAL
Active ingredient(s)LISINOPRIL
Strength5 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Marketing categoryANDA

Packages

68071-3123-1 — 120 TABLET in 1 BOTTLE (68071-3123-1)

68071-3123-3 — 30 TABLET in 1 BOTTLE (68071-3123-3)

68071-3123-6 — 60 TABLET in 1 BOTTLE (68071-3123-6)

68071-3123-9 — 90 TABLET in 1 BOTTLE (68071-3123-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2183 — Lisinopril and Hydrochlorothiazide, 68071-2224 — Lisinopril, 68071-2263 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2291 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2303 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2740 — Lisinopril and Hydrochlorothiazide Tablets, 68071-3008 — Lisinopril and hydrochlorothiazide, 68071-3043 — Lisinopril, 68071-3064 — Lisinopril, 68071-3122 — Lisinopril, 68071-3177 — Lisinopril and Hydrochlorothiazide, 68071-3178 — Lisinopril, 68071-3220 — Lisinopril, 68071-3409 — Lisinopril, 68071-3411 — Lisinopril, 68071-4435 — Lisinopril and Hydrochlorothiazide, 68071-4660 — Lisinopril, 68071-4858 — Lisinopril, 68071-5036 — Lisinopril, 68071-5046 — Lisinopril, +342 more

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