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HYDROCHLOROTHIAZIDE

NDC 60760-662 · St. Mary's Medical Park Pharmacy

Generic nameHYDROCHLOROTHIAZIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE
Strength12.5 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

60760-662-90 — 90 TABLET in 1 BOTTLE, PLASTIC (60760-662-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60505-2656 — Triamterene and Hydrochlorothiazide, 60505-2657 — Triamterene and Hydrochlorothiazide, 60687-593 — 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, 60760-783 — Triamterene and Hydrochlorothiazide, 62135-448 — Hydrochlorothiazide, 62135-449 — Hydrochlorothiazide, 62135-529 — TRIAMTERENE AND HYDROCHLOROTHIAZIDE, 62135-667 — Quinapril and Hydrochlorothiazide, 62135-668 — Quinapril and Hydrochlorothiazide, 62135-669 — Quinapril and Hydrochlorothiazide, 62135-738 — Hydrochlorothiazide, 62332-048 — Losartan Potassium and Hydrochlorothiazide, 62332-049 — Losartan Potassium 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.