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Lisinopril and Hydrochlorothiazide

NDC 68645-557 · Legacy Pharmaceutical Packaging, LLC

Generic nameLisinopril and Hydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE, LISINOPRIL
Strength12.5; 20 mg/1; mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

68645-557-54 — 30 TABLET in 1 BOTTLE (68645-557-54)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68462-578 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-579 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-840 — Telmisartan and Hydrochlorothiazide, 68462-841 — Telmisartan and Hydrochlorothiazide, 68462-842 — Telmisartan and Hydrochlorothiazide, 68462-878 — Bisoprolol Fumarate and Hydrochlorothiazide, 68462-879 — Bisoprolol Fumarate and Hydrochlorothiazide, 68462-880 — Bisoprolol Fumarate and Hydrochlorothiazide, 68645-510 — Hydrochlorothiazide, 68645-556 — Lisinopril and Hydrochlorothiazide, 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, 68788-6452 — Losartan Potassium and Hydrochlorothiazide, 68788-6820 — Lisinopril, +1122 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.