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Valsartan and Hydrochlorothiazide

NDC 71205-015 · Proficient Rx LP

Generic nameValsartan and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VALSARTAN, HYDROCHLOROTHIAZIDE
Strength25; 320 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

71205-015-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-015-30)

71205-015-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-015-60)

71205-015-90 — 90 TABLET, FILM COATED in 1 BOTTLE (71205-015-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70771-1922 — sacubitril and valsartan, 70771-1923 — sacubitril and valsartan, 70954-310 — Valsartan, 70954-412 — Bisoprolol Fumarate and Hydrochlorothiazide, 70954-413 — Bisoprolol Fumarate and Hydrochlorothiazide, 70954-414 — Bisoprolol Fumarate and Hydrochlorothiazide, 70954-522 — hydrochlorothiazide, 70954-975 — Sacubitril and Valsartan, 70954-976 — Sacubitril and Valsartan, 70954-977 — Sacubitril and Valsartan, 71205-022 — Lisinopril and Hydrochlorothiazide, 71205-042 — Valsartan and Hydrochlorothiazide, 71205-063 — Irbesartan and Hydrochlorothiazide, 71205-090 — Hydrochlorothiazide, 71205-161 — hydrochlorothiazide, 71205-249 — Valsartan and Hydrochlorothiazide, 71205-258 — Valsartan and Hydrochlorothiazide, 71205-301 — Valsartan, 71205-327 — Valsartan and Hydrochlorothiazide, 71205-419 — 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.