NDC 51672-4031 – Warfarin Sodium

Warfarin Sodium 4 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC51672-4031

Product details

Brand name
Warfarin Sodium
Generic name
Warfarin Sodium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040301
Marketed since
July 15, 1999
Listing expires
December 31, 2026
Pharmacologic class
Vitamin K Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Warfarin Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
51672-4031-1100 TABLET in 1 BOTTLE (51672-4031-1)Jul 15, 1999
51672-4031-31000 TABLET in 1 BOTTLE (51672-4031-3)Jul 15, 1999
51672-4031-75000 TABLET in 1 BOTTLE (51672-4031-7)Jul 15, 1999

Recalls mentioning this NDC

Other Warfarin Sodium products