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Fosinopril Sodium and Hydrochlorothiazide

NDC 69097-972 · CIPLA USA INC.

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

69097-972-07 — 100 TABLET in 1 BOTTLE (69097-972-07)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-9809 — LISINOPRIL AND HYDROCHLOROTHIAZIDE, 69097-828 — quinapril and Hydrochlorothiazide 10/12.5, 69097-829 — Quinapril and Hydrochlorothiazide 20/12.5, 69097-831 — Quinapril and Hydrochlorothiazide 20/25, 69097-856 — Fosinopril, 69097-857 — Fosinopril, 69097-858 — Fosinopril, 69097-968 — Lisinopril and Hydrochlorothiazide Tablets, 69097-969 — Lisinopril and Hydrochlorothiazide Tablets, 69097-971 — Lisinopril and Hydrochlorothiazide Tablets, 69097-973 — Fosinopril Sodium and Hydrochlorothiazide, 69315-130 — HYDROCHLOROTHIAZIDE, 69315-131 — HYDROCHLOROTHIAZIDE, 69315-155 — HYDROCHLOROTHIAZIDE, 69367-219 — Hydrochlorothiazide, 69584-361 — Hydrochlorothiazide, 69584-362 — Hydrochlorothiazide, 70010-187 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-188 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-189 — LOSARTAN POTASSIUM 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.