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Lisinopril

NDC 72789-093 · PD-Rx Pharmaceuticals, Inc.

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

72789-093-30 — 30 TABLET in 1 BOTTLE, PLASTIC (72789-093-30)

72789-093-90 — 90 TABLET in 1 BOTTLE, PLASTIC (72789-093-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-726 — Lisinopril, 71610-727 — LISINOPRIL, 71610-731 — LISINOPRIL, 71610-733 — LISINOPRIL, 71610-741 — Lisinopril, 71610-748 — LISINOPRIL, 71610-766 — LISINOPRIL, 71610-838 — Lisinopril and Hydrochlorothiazide, 71610-868 — Lisinopril and Hydrochlorothiazide Tablets, 72189-651 — Lisinopril/HCTZ, 72789-101 — Lisinopril, 72865-208 — Lisinopril, 72865-209 — Lisinopril, 72865-210 — Lisinopril, 72865-211 — Lisinopril, 72865-212 — Lisinopril, 72865-213 — Lisinopril, 76282-417 — lisinopril, 76282-418 — lisinopril, 76282-419 — 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.