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Losartan Potassium and Hydrochlorothiazide

NDC 68071-4159 · NuCare Pharmaceuticals,Inc.

Generic nameLosartan Potassium and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LOSARTAN POTASSIUM, HYDROCHLOROTHIAZIDE
Strength12.5; 100 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

68071-4159-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68071-4159-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2690 — Losartan potassium, 68071-2740 — Lisinopril and Hydrochlorothiazide Tablets, 68071-3008 — Lisinopril and hydrochlorothiazide, 68071-3177 — Lisinopril and Hydrochlorothiazide, 68071-3323 — Hydrochlorothiazide, 68071-3443 — Hydrochlorothiazide, 68071-3608 — HYDROCHLOROTHIAZIDE, 68071-3652 — HYDROCHLOROTHIAZIDE, 68071-3846 — Losartan Potassium, 68071-3879 — Triamterene and Hydrochlorothiazide, 68071-4435 — Lisinopril and Hydrochlorothiazide, 68071-4471 — Losartan Potassium, 68071-4518 — Losartan Potassium and Hydrochlorothiazide, 68071-4687 — Triamterene and Hydrochlorothiazide, 68071-4819 — Hydrochlorothiazide, 68071-4933 — Hydrochlorothiazide, 68071-4943 — Losartan Potassium, 68071-4963 — Hydrochlorothiazide, 68071-5040 — Losartan Potassium, 68071-5041 — Losartan Potassium, +1060 more

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