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Hydrochlorothiazide

NDC 66267-106 · 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

66267-106-30 — 30 TABLET in 1 BOTTLE (66267-106-30)

66267-106-60 — 60 TABLET in 1 BOTTLE (66267-106-60)

66267-106-90 — 90 TABLET in 1 BOTTLE (66267-106-90)

66267-106-91 — 120 TABLET in 1 BOTTLE (66267-106-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-780 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-781 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-837 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-838 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-976 — Telmisartan and Hydrochlorothiazide, 65862-977 — Telmisartan and Hydrochlorothiazide, 65862-978 — Telmisartan and Hydrochlorothiazide, 66993-188 — spironolactone and hydrochlorothiazide, 67046-0433 — Lisinopril and Hydrochlorothiazide, 67046-1618 — Losartan Potassium and Hydrochlorothiazide, 67046-1664 — Hydrochlorothiazide, 67296-2043 — Hydrochlorothiazide, 67296-2280 — Hydrochlorothiazide, 67544-739 — Hydrochlorothiazide, 67877-451 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 67877-452 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 67877-453 — 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.