Digoxin

NDC 51655-403 · Northwind Health Company, LLC

Generic nameDigoxin

Dosage formTABLET

RouteORAL

Active ingredient(s)DIGOXIN

Strength.125 mg/1

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

Marketing categoryANDA

Packages

51655-403-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-403-52)

FDA lists these products with the same active ingredient.

0904-5922 — Digoxin, 10135-747 — Digoxin, 10135-748 — Digoxin, 17856-0057 — Digoxin, 50090-5642 — Digoxin, 50090-5862 — Digoxin, 50090-6588 — Digoxin, 50090-6708 — Digoxin, 50090-7865 — Digoxin, 50268-238 — Digoxin, 51662-1217 — DIGOXIN, 55154-5106 — Digoxin, 55154-5882 — Digoxin, 59212-240 — digoxin, 59212-242 — digoxin, 59212-249 — digoxin, 59651-436 — Digoxin, 59651-437 — Digoxin, 59651-438 — Digoxin, 60429-100 — 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.