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Fosinopril Sodium

NDC 65862-471 · Aurobindo Pharma Limited

Generic nameFosinopril Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)FOSINOPRIL SODIUM
Strength10 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Marketing categoryANDA

Packages

65862-471-30 — 30 TABLET in 1 BOTTLE (65862-471-30)

65862-471-90 — 90 TABLET in 1 BOTTLE (65862-471-90)

65862-471-99 — 1000 TABLET in 1 BOTTLE (65862-471-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-386 — fosinopirl sodium, 43547-387 — fosinopril sodium, 43547-388 — fosinopril sodium, 50090-2977 — Fosinopril, 50090-4743 — fosinopril sodium, 62135-041 — Fosinopril Sodium, 62135-042 — Fosinopril Sodium, 62135-043 — Fosinopril Sodium, 65862-308 — Fosinopril Sodium and Hydrochlorothiazide, 65862-309 — Fosinopril Sodium and Hydrochlorothiazide, 65862-472 — Fosinopril Sodium, 65862-473 — Fosinopril Sodium, 69097-856 — Fosinopril, 69097-857 — Fosinopril, 69097-858 — Fosinopril, 69097-972 — Fosinopril Sodium and Hydrochlorothiazide, 69097-973 — Fosinopril Sodium and Hydrochlorothiazide, 71335-0187 — Fosinopril, 71335-0381 — Fosinopril, 71335-0726 — fosinopirl sodium, +4 more

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