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Fosinopril Sodium and Hydrochlorothiazide

NDC 65862-308 · Aurobindo Pharma Limited

Generic nameFosinopril Sodium and Hydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)FOSINOPRIL SODIUM, HYDROCHLOROTHIAZIDE
Strength10; 12.5 mg/1; mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

65862-308-01 — 100 TABLET in 1 BOTTLE (65862-308-01)

65862-308-30 — 30 TABLET in 1 BOTTLE (65862-308-30)

65862-308-99 — 1000 TABLET in 1 BOTTLE (65862-308-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65162-849 — Valsartan and Hydrochlorothiazide, 65862-043 — Lisinopril and Hydrochlorothiazide, 65862-044 — Lisinopril and Hydrochlorothiazide, 65862-045 — Lisinopril and Hydrochlorothiazide, 65862-113 — Hydrochlorothiazide, 65862-133 — Hydrochlorothiazide, 65862-134 — Hydrochlorothiazide, 65862-161 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-162 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-163 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-309 — Fosinopril Sodium and Hydrochlorothiazide, 65862-468 — Losartan Potassium and Hydrochlorothiazide, 65862-469 — Losartan Potassium and Hydrochlorothiazide, 65862-470 — Losartan Potassium and Hydrochlorothiazide, 65862-471 — Fosinopril Sodium, 65862-472 — Fosinopril Sodium, 65862-473 — Fosinopril Sodium, 65862-547 — Valsartan and Hydrochlorothiazide, 65862-548 — Valsartan and Hydrochlorothiazide, 65862-549 — Valsartan and Hydrochlorothiazide, +875 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.