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Lisinopril

NDC 63629-1761 · Bryant Ranch Prepack

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

63629-1761-1 — 30 TABLET in 1 BOTTLE (63629-1761-1)

63629-1761-2 — 90 TABLET in 1 BOTTLE (63629-1761-2)

63629-1761-3 — 60 TABLET in 1 BOTTLE (63629-1761-3)

63629-1761-4 — 100 TABLET in 1 BOTTLE (63629-1761-4)

63629-1761-5 — 10 TABLET in 1 BOTTLE (63629-1761-5)

63629-1761-6 — 28 TABLET in 1 BOTTLE (63629-1761-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-237 — Lisinopril, 63187-257 — Lisinopril, 63187-319 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 63187-442 — Lisinopril, 63187-467 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 63187-534 — Lisinopril, 63187-775 — Lisinopril, 63187-780 — Lisinopril, 63187-821 — Lisinopril, 63187-825 — Lisinopril, 63629-3739 — Lisinopril and Hydrochlorothiazide, 63629-4470 — Lisinopril and Hydrochlorothiazide, 63629-5247 — Lisinopril, 63629-5382 — Lisinopril, 63629-8736 — Lisinopril, 63629-8823 — Lisinopril, 65862-037 — Lisinopril, 65862-038 — Lisinopril, 65862-039 — Lisinopril, 65862-040 — 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.