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Lisinopril

NDC 68001-335 · BluePoint Laboratories

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

68001-335-00 — 100 TABLET in 1 BOTTLE (68001-335-00)

68001-335-08 — 1000 TABLET in 1 BOTTLE (68001-335-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-045 — Lisinopril and Hydrochlorothiazide, 67046-0422 — Lisinopril, 67046-0423 — Lisinopril, 67046-0433 — Lisinopril and Hydrochlorothiazide, 67046-0858 — Lisinopril, 67046-2097 — Lisinopril, 67296-1202 — LISINOPRIL, 68001-332 — Lisinopril, 68001-333 — Lisinopril, 68001-334 — Lisinopril, 68001-336 — Lisinopril, 68001-486 — Lisinopril, 68071-1672 — Lisinopril, 68071-1775 — 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, +342 more

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