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Hydrochlorothiazide

NDC 68071-4933 · NuCare Pharmaceuticals,Inc.

Generic nameHydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE
Strength25 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

68071-4933-7 — 20 TABLET in 1 BOTTLE (68071-4933-7)

68071-4933-9 — 90 TABLET in 1 BOTTLE (68071-4933-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3323 — Hydrochlorothiazide, 68071-3443 — Hydrochlorothiazide, 68071-3608 — HYDROCHLOROTHIAZIDE, 68071-3652 — HYDROCHLOROTHIAZIDE, 68071-3879 — Triamterene and Hydrochlorothiazide, 68071-4159 — Losartan Potassium and Hydrochlorothiazide, 68071-4435 — Lisinopril and Hydrochlorothiazide, 68071-4518 — Losartan Potassium and Hydrochlorothiazide, 68071-4687 — Triamterene and Hydrochlorothiazide, 68071-4819 — Hydrochlorothiazide, 68071-4963 — Hydrochlorothiazide, 68071-5211 — Hydrochlorothiazide, 68084-750 — Triamterene and Hydrochlorothiazide, 68180-101 — Valsartan and Hydrochlorothiazide, 68180-102 — Valsartan and Hydrochlorothiazide, 68180-103 — Valsartan and Hydrochlorothiazide, 68180-104 — Valsartan and Hydrochlorothiazide, 68180-105 — Valsartan and Hydrochlorothiazide, 68180-193 — Telmisartan and Hydrochlorothiazide, 68180-194 — Telmisartan 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.