Digoxin

NDC 70954-200 · ANI Pharmaceuticals, Inc.

Generic nameDigoxin

Dosage formTABLET

RouteORAL

Active ingredient(s)DIGOXIN

Strength.0625 mg/1

Pharmacologic classCardiac Glycoside [EPC], Cardiac Glycosides [CS]

Marketing categoryANDA

Packages

70954-200-10 — 100 TABLET in 1 BOTTLE (70954-200-10)

FDA lists these products with the same active ingredient.

67046-1317 — Digoxin, 69238-1991 — Digoxin, 69238-1992 — Digoxin, 69292-605 — Digoxin, 70515-260 — digoxin, 70515-261 — digoxin, 70515-262 — digoxin, 70515-263 — digoxin, 70518-3859 — Digoxin, 70518-3860 — 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, 72162-2269 — 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.