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LISINOPRIL

NDC 68071-3220 · NuCare Pharmaceuticals, Inc.

Generic nameLisinopril
Dosage formTABLET
RouteORAL
Active ingredient(s)LISINOPRIL
Strength40 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Marketing categoryANDA

Packages

68071-3220-1 — 100 TABLET in 1 BOTTLE (68071-3220-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-3123 — Lisinopril, 68071-3177 — Lisinopril and Hydrochlorothiazide, 68071-3178 — Lisinopril, 68071-3409 — Lisinopril, 68071-3411 — Lisinopril, 68071-4435 — Lisinopril and Hydrochlorothiazide, 68071-4660 — Lisinopril, 68071-4858 — Lisinopril, 68071-5036 — Lisinopril, 68071-5046 — Lisinopril, 68071-5089 — Lisinopril, 68071-5098 — Lisinopril, 68071-5143 — 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.