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Lisinopril

NDC 31722-176 · Camber Pharmaceuticals, Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

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

31722-176-31 — 95238 TABLET in 1 CARTON (31722-176-31)

31722-176-01 — 100 TABLET in 1 BOTTLE (31722-176-01)

31722-176-10 — 1000 TABLET in 1 BOTTLE (31722-176-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-879 — lisinopril, 23155-880 — lisinopril, 23155-881 — lisinopril, 24979-238 — Lisinopril, 24979-239 — Lisinopril, 24979-240 — Lisinopril, 24979-241 — Lisinopril, 24979-242 — Lisinopril, 24979-243 — Lisinopril, 31722-172 — Lisinopril, 31722-177 — Lisinopril, 31722-178 — Lisinopril, 31722-179 — Lisinopril, 31722-180 — Lisinopril, 42708-031 — Lisinopril, 42708-032 — Lisinopril, 42708-033 — Lisinopril, 42708-034 — Lisinopril and Hydrochlorothiazide, 42708-094 — Lisinopril, 42708-096 — 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.