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Lisinopril

NDC 68645-609 · Legacy Pharmaceutical Packaging, LLC

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

68645-609-90 — 90 TABLET in 1 BOTTLE (68645-609-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-519 — Lisinopril and Hydrochlorothiazide, 68180-520 — Lisinopril and Hydrochlorothiazide, 68180-979 — Lisinopril, 68180-980 — Lisinopril, 68180-981 — Lisinopril, 68180-982 — Lisinopril, 68645-556 — Lisinopril and Hydrochlorothiazide, 68645-557 — Lisinopril and Hydrochlorothiazide, 68645-558 — Lisinopril and Hydrochlorothiazide, 68645-608 — Lisinopril, 68645-610 — Lisinopril, 68645-611 — Lisinopril, 68645-612 — Lisinopril, 68645-613 — Lisinopril, 68788-6407 — Lisinopril, 68788-6820 — Lisinopril, 68788-6920 — Lisinopril, 68788-7012 — Lisinopril, 68788-8224 — Lisinopril and Hydrochlorothiazide Tablets, 68788-8241 — 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.