NDC 51672-4228 – Rivaroxaban

Rivaroxaban 2.5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC51672-4228

Product details

Brand name
Rivaroxaban
Generic name
Rivaroxaban
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208557
Marketed since
October 15, 2025
Listing expires
December 31, 2027
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Rivaroxaban →

Package NDC codes (2)

Package NDCDescriptionSince
51672-4228-460 TABLET, COATED in 1 BOTTLE (51672-4228-4)Oct 15, 2025
51672-4228-9180 TABLET, COATED in 1 BOTTLE (51672-4228-9)Oct 15, 2025

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