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Hydrochlorothiazide

NDC 69584-362 · Oxford Pharmaceuticals, LLC

Generic nameHydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE
Strength50 mg/1
Pharmacologic classIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

69584-362-10 — 100 TABLET in 1 BOTTLE (69584-362-10)

69584-362-90 — 1000 TABLET in 1 BOTTLE (69584-362-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69097-968 — Lisinopril and Hydrochlorothiazide Tablets, 69097-969 — Lisinopril and Hydrochlorothiazide Tablets, 69097-971 — Lisinopril and Hydrochlorothiazide Tablets, 69097-972 — Fosinopril Sodium and Hydrochlorothiazide, 69097-973 — Fosinopril Sodium and Hydrochlorothiazide, 69315-130 — HYDROCHLOROTHIAZIDE, 69315-131 — HYDROCHLOROTHIAZIDE, 69315-155 — HYDROCHLOROTHIAZIDE, 69367-219 — Hydrochlorothiazide, 69584-361 — Hydrochlorothiazide, 70010-187 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-188 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-189 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70436-014 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-015 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-016 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-017 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-018 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70518-0174 — Lisinopril and Hydrochlorothiazide, 70518-0196 — Lisinopril 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.