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Hydrochlorothiazide

NDC 70518-4113 · REMEDYREPACK 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

70518-4113-0 — 30 TABLET in 1 BLISTER PACK (70518-4113-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-1662 — Triamterene and Hydrochlorothiazide, 70518-2269 — Olmesartan Medoxomil and Hydrochlorothiazide, 70518-2550 — Hydrochlorothiazide, 70518-2737 — Losartan Potassium and Hydrochlorothiazide, 70518-3398 — losartan potassium and hydrochlorothiazide, 70518-3404 — losartan potassium and hydrochlorothiazide, 70518-3420 — losartan potassium and hydrochlorothiazide, 70518-3505 — Lisinopril and Hydrochlorothiazide Tablets, 70518-3749 — Hydrochlorothiazide, 70518-3780 — hydrochlorothiazide, 70518-4165 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 70518-4251 — hydrochlorothiazide, 70518-4270 — Triamterene and Hydrochlorothiazide, 70518-4351 — Triamterene and Hydrochlorothiazide, 70518-4359 — hydrochlorothiazide, 70518-4466 — HYDROCHLOROTHIAZIDE, 70518-4516 — Lisinopril and Hydrochlorothiazide Tablets, 70518-4517 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 70518-4525 — hydrochlorothiazide, 70518-4577 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels