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LISINOPRIL

NDC 68071-1775 · NuCare Pharmaceuticals,Inc.

Generic nameLisinopril
Dosage formTABLET
RouteORAL
Active ingredient(s)LISINOPRIL
Strength20 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Marketing categoryANDA

Packages

68071-1775-1 — 100 TABLET in 1 BOTTLE (68071-1775-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-0858 — Lisinopril, 67046-2097 — Lisinopril, 67296-1202 — LISINOPRIL, 68001-332 — Lisinopril, 68001-333 — Lisinopril, 68001-334 — Lisinopril, 68001-335 — Lisinopril, 68001-336 — Lisinopril, 68001-486 — Lisinopril, 68071-1672 — Lisinopril, 68071-1894 — Lisinopril, 68071-1945 — Lisinopril and Hydrochlorothiazide, 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, +342 more

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