DIGOXIN

NDC 51662-1217 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameDIGOXIN

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)DIGOXIN

Strength.25 mg/mL

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

Marketing categoryANDA

Packages

51662-1217-1 — 2 mL in 1 AMPULE (51662-1217-1)

51662-1217-3 — 25 POUCH in 1 CASE (51662-1217-3) / 1 mL in 1 POUCH (51662-1217-2)

J1160 — Injection, digoxin, up to 0.5 mg Medicare Part B payment limit (ASP + 6%): $3.91

FDA lists these products with the same active ingredient.

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, 51655-403 — 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, 60687-858 — 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.