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Hydrochlorothiazide

NDC 60687-593 · American Health Packaging

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

Packages

60687-593-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-593-01) / 1 TABLET in 1 BLISTER PACK (60687-593-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55700-006 — Hydrochlorothiazide, 57237-002 — Hydrochlorothiazide, 59651-678 — Bisoprolol Fumarate and Hydrochlorothiazide, 59651-679 — Bisoprolol Fumarate and Hydrochlorothiazide, 59651-680 — Bisoprolol Fumarate and Hydrochlorothiazide, 59746-337 — losartan potassium and hydrochlorothiazide, 59746-338 — losartan potassium and hydrochlorothiazide, 59746-339 — losartan potassium and hydrochlorothiazide, 60505-2656 — Triamterene and Hydrochlorothiazide, 60505-2657 — Triamterene and Hydrochlorothiazide, 60687-683 — hydrochlorothiazide, 60687-894 — Hydrochlorothiazide, 60760-063 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 60760-315 — Hydrochlorothiazide, 60760-519 — Lisinopril and Hydrochlorothiazide Tablets, 60760-572 — losartan potassium and hydrochlorothiazide, 60760-586 — Lisinopril and Hydrochlorothiazide Tablets, 60760-662 — HYDROCHLOROTHIAZIDE, 60760-783 — Triamterene and Hydrochlorothiazide, 62135-448 — 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.