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Hydrochlorothiazide

NDC 87441-038 · Unit Dose Solutions, 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

87441-038-01 — 30 TABLET in 1 BLISTER PACK (87441-038-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

78206-139 — losartan potassium and hydrochlorothiazide, 78206-140 — losartan potassium and hydrochlorothiazide, 78206-141 — losartan potassium and hydrochlorothiazide, 80425-0207 — Lisinopril and Hydrochlorothiazide, 82804-031 — Hydrochlorothiazide, 82804-103 — losartan potassium and hydrochlorothiazide, 82804-239 — losartan potassium and hydrochlorothiazide, 82804-307 — Lisinopril and Hydrochlorothiazide Tablets, 82804-308 — Triamterene and Hydrochlorothiazide, 82804-972 — Hydrochlorothiazide, 82804-973 — Hydrochlorothiazide, 82868-006 — Triamterene and Hydrochlorothiazide, 82868-016 — hydrochlorothiazide, 82868-022 — Triamterene and Hydrochlorothiazide, 82868-032 — Triamterene and Hydrochlorothiazide, 82868-054 — Valsartan and Hydrochlorothiazide, 83008-086 — losartan potassium and hydrochlorothiazide, 84677-056 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 84677-057 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 84677-058 — OLMESARTAN MEDOXOMIL 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.