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LISINOPRIL

NDC 68788-7012 · Preferred Pharmaceuticals 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

68788-7012-1 — 100 TABLET in 1 BOTTLE (68788-7012-1)

68788-7012-3 — 30 TABLET in 1 BOTTLE (68788-7012-3)

68788-7012-6 — 60 TABLET in 1 BOTTLE (68788-7012-6)

68788-7012-9 — 90 TABLET in 1 BOTTLE (68788-7012-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68645-558 — Lisinopril and Hydrochlorothiazide, 68645-608 — Lisinopril, 68645-609 — Lisinopril, 68645-610 — Lisinopril, 68645-611 — Lisinopril, 68645-612 — Lisinopril, 68645-613 — Lisinopril, 68788-6407 — Lisinopril, 68788-6820 — Lisinopril, 68788-6920 — Lisinopril, 68788-8224 — Lisinopril and Hydrochlorothiazide Tablets, 68788-8241 — Lisinopril and Hydrochlorothiazide Tablets, 68788-8253 — Lisinopril and Hydrochlorothiazide Tablets, 68788-8562 — Lisinopril, 68788-9807 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 68788-9808 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 68788-9809 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 69097-968 — Lisinopril and Hydrochlorothiazide Tablets, 69097-969 — Lisinopril and Hydrochlorothiazide Tablets, 69097-971 — 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.