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Valsartan and Hydrochlorothiazide

NDC 68180-103 · Lupin Pharmaceuticals, Inc.

Generic nameValsartan and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE, VALSARTAN
Strength12.5; 80 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4435 — Lisinopril and Hydrochlorothiazide, 68071-4518 — Losartan Potassium and Hydrochlorothiazide, 68071-4687 — Triamterene and Hydrochlorothiazide, 68071-4819 — Hydrochlorothiazide, 68071-4933 — Hydrochlorothiazide, 68071-4963 — Hydrochlorothiazide, 68071-5211 — Hydrochlorothiazide, 68084-750 — Triamterene and Hydrochlorothiazide, 68180-101 — Valsartan and Hydrochlorothiazide, 68180-102 — Valsartan and Hydrochlorothiazide, 68180-104 — Valsartan and Hydrochlorothiazide, 68180-105 — Valsartan and Hydrochlorothiazide, 68180-193 — Telmisartan and Hydrochlorothiazide, 68180-194 — Telmisartan and Hydrochlorothiazide, 68180-195 — Telmisartan and Hydrochlorothiazide, 68180-215 — Losartan Potassium and Hydrochlorothiazide, 68180-216 — Losartan Potassium and Hydrochlorothiazide, 68180-217 — Losartan Potassium and Hydrochlorothiazide, 68180-276 — Valsartan, 68180-518 — Lisinopril and Hydrochlorothiazide, +1132 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