Digoxin

NDC 71335-3156 · 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

71335-3156-1 — 30 TABLET in 1 BOTTLE (71335-3156-1)

71335-3156-2 — 60 TABLET in 1 BOTTLE (71335-3156-2)

71335-3156-3 — 90 TABLET in 1 BOTTLE (71335-3156-3)

71335-3156-4 — 100 TABLET in 1 BOTTLE (71335-3156-4)

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, 71335-9610 — Digoxin, 71610-019 — digoxin, 71872-7325 — Digoxin, 72162-2268 — Digoxin, 72162-2269 — 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.