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Lisinopril

NDC 42708-176 · QPharma, 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

42708-176-30 — 30 TABLET in 1 BOTTLE, PLASTIC (42708-176-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42708-031 — Lisinopril, 42708-032 — Lisinopril, 42708-033 — Lisinopril, 42708-034 — Lisinopril and Hydrochlorothiazide, 42708-094 — Lisinopril, 42708-096 — Lisinopril, 42708-142 — Lisinopril, 42708-150 — Lisinopril and Hydrochlorothiazide, 42708-154 — Lisinopril, 42708-165 — Lisinopril, 43063-074 — Lisinopril, 43063-458 — Lisinopril and Hydrochlorothiazide, 43063-468 — Lisinopril and Hydrochlorothiazide, 43063-482 — Lisinopril and Hydrochlorothiazide, 43063-769 — Lisinopril, 43063-786 — Lisinopril, 43063-800 — Lisinopril, 43063-810 — Lisinopril, 43063-811 — Lisinopril, 43063-812 — 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.