NDC 71335-3156 – Digoxin

Digoxin 250 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3156

Product details

Brand name
Digoxin
Generic name
Digoxin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076268
Marketed since
September 1, 2022
Listing expires
December 31, 2027
Pharmacologic class
Cardiac Glycoside

Active ingredients

Uses, dosage, side effects and warnings for Digoxin →

Package NDC codes (4)

Package NDCDescriptionSince
71335-3156-130 TABLET in 1 BOTTLE (71335-3156-1)Jul 27, 2026
71335-3156-260 TABLET in 1 BOTTLE (71335-3156-2)Jul 27, 2026
71335-3156-390 TABLET in 1 BOTTLE (71335-3156-3)Jul 27, 2026
71335-3156-4100 TABLET in 1 BOTTLE (71335-3156-4)Jul 27, 2026

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