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Triamterene and Hydrochlorothiazide

NDC 68382-855 · Zydus Pharmaceuticals (USA) Inc.

Generic nameTriamterene and Hydrochlorothiazide
Dosage formCAPSULE
RouteORAL
Active ingredient(s)TRIAMTERENE, HYDROCHLOROTHIAZIDE
Strength25; 37.5 mg/1; mg/1
Pharmacologic classDecreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

68382-855-01 — 100 CAPSULE in 1 BOTTLE (68382-855-01)

68382-855-05 — 500 CAPSULE in 1 BOTTLE (68382-855-05)

68382-855-10 — 1000 CAPSULE in 1 BOTTLE (68382-855-10)

68382-855-77 — 10 BLISTER PACK in 1 CARTON (68382-855-77) / 10 CAPSULE in 1 BLISTER PACK (68382-855-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-216 — Losartan Potassium and Hydrochlorothiazide, 68180-217 — Losartan Potassium and Hydrochlorothiazide, 68180-518 — Lisinopril and Hydrochlorothiazide, 68180-519 — Lisinopril and Hydrochlorothiazide, 68180-520 — Lisinopril and Hydrochlorothiazide, 68180-771 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-772 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-773 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-774 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-775 — Amlodipine, Valsartan and Hydrochlorothiazide, 68382-856 — triamterene and hydrochlorothiazide, 68382-857 — triamterene and hydrochlorothiazide, 68462-576 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-577 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-578 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-579 — Benazepril Hydrochloride and Hydrochlorothiazide, 68462-840 — Telmisartan and Hydrochlorothiazide, 68462-841 — Telmisartan and Hydrochlorothiazide, 68462-842 — Telmisartan and Hydrochlorothiazide, 68462-878 — Bisoprolol Fumarate and Hydrochlorothiazide, +863 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