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Hydrochlorothiazide

NDC 71205-589 · Proficient Rx LP

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

Packages

71205-589-30 — 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-589-30)

71205-589-60 — 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-589-60)

71205-589-90 — 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-589-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-015 — Valsartan and Hydrochlorothiazide, 71205-022 — Lisinopril and Hydrochlorothiazide, 71205-042 — Valsartan and Hydrochlorothiazide, 71205-063 — Irbesartan and Hydrochlorothiazide, 71205-090 — Hydrochlorothiazide, 71205-161 — hydrochlorothiazide, 71205-249 — Valsartan and Hydrochlorothiazide, 71205-258 — Valsartan and Hydrochlorothiazide, 71205-327 — Valsartan and Hydrochlorothiazide, 71205-419 — Hydrochlorothiazide, 71205-751 — Hydrochlorothiazide, 71205-763 — Lisinopril and Hydrochlorothiazide Tablets, 71205-793 — hydrochlorothiazide, 71205-980 — Hydrochlorothiazide, 71335-0067 — hydrochlorothiazide, 71335-0145 — Hydrochlorothiazide, 71335-0152 — Losartan Potassium and Hydrochlorothiazide, 71335-0269 — Hydrochlorothiazide, 71335-0326 — Triamterene and Hydrochlorothiazide, 71335-0356 — Triamterene 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.