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Hydrochlorothiazide

NDC 50228-111 · ScieGen 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

50228-111-10 — 1000 TABLET in 1 BOTTLE (50228-111-10)

50228-111-30 — 30 TABLET in 1 BOTTLE (50228-111-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7478 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 50090-7571 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 50090-7664 — Losartan Potassium and Hydrochlorothiazide, 50090-7751 — Lisinopril and Hydrochlorothiazide, 50090-7764 — hydrochlorothiazide, 50090-7765 — hydrochlorothiazide, 50090-7772 — Hydrochlorothiazide, 50090-7773 — Hydrochlorothiazide, 50090-7817 — HYDROCHLOROTHIAZIDE, 50090-7821 — Losartan Potassium and Hydrochlorothiazide, 50228-112 — Hydrochlorothiazide, 50228-146 — Hydrochlorothiazide, 50228-147 — valsartan and hydrochlorothiazide, 50228-148 — valsartan and hydrochlorothiazide, 50228-149 — valsartan and hydrochlorothiazide, 50228-150 — valsartan and hydrochlorothiazide, 50228-151 — valsartan and hydrochlorothiazide, 50228-342 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 50228-343 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 50228-344 — 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