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Digoxin

NDC 72162-2269 · Bryant Ranch Prepack

Generic nameDigoxin
Dosage formTABLET
RouteORAL
Active ingredient(s)DIGOXIN
Strength250 ug/1
Pharmacologic classCardiac Glycoside [EPC], Cardiac Glycosides [CS]
Marketing categoryANDA

Packages

72162-2269-0 — 1000 TABLET in 1 BOTTLE (72162-2269-0)

72162-2269-1 — 100 TABLET in 1 BOTTLE (72162-2269-1)

72162-2269-2 — 1000 TABLET in 1 BOTTLE (72162-2269-2)

72162-2269-4 — 100 TABLET in 1 BOTTLE (72162-2269-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70515-260 — digoxin, 70515-261 — digoxin, 70515-262 — digoxin, 70515-263 — digoxin, 70518-3859 — Digoxin, 70518-3860 — Digoxin, 70954-200 — Digoxin, 70954-201 — Digoxin, 70954-202 — Digoxin, 71335-2463 — Digoxin, 71335-2464 — Digoxin, 71335-3156 — Digoxin, 71335-9610 — Digoxin, 71610-019 — digoxin, 71872-7325 — Digoxin, 72162-2268 — Digoxin, 82685-201 — Digoxin, 82685-202 — Digoxin, 82804-244 — Digoxin, 84549-410 — Digoxin, +39 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.