Skip to main content

Hydrochlorothiazide

NDC 68071-2405 · NuCare Pharmaceuticals,Inc.

Generic nameHydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE
Strength50 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

68071-2405-1 — 100 TABLET in 1 BOTTLE (68071-2405-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-328 — Triamterene and Hydrochlorothiazide, 68001-387 — Triamterene and Hydrochlorothiazide, 68001-388 — Triamterene and Hydrochlorothiazide, 68071-1834 — Triamterene and Hydrochlorothiazide, 68071-1945 — Lisinopril and Hydrochlorothiazide, 68071-2183 — Lisinopril and Hydrochlorothiazide, 68071-2263 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2291 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2303 — Lisinopril and Hydrochlorothiazide Tablets, 68071-2371 — Triamterene and Hydrochlorothiazide, 68071-2411 — Hydrochlorothiazide, 68071-2533 — Triamterene and Hydrochlorothiazide, 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, 68071-3879 — Triamterene and Hydrochlorothiazide, +854 more

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