NDC 50090-3639 – Xarelto

Rivaroxaban 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-3639

Product details

Brand name
Xarelto
Generic name
Rivaroxaban
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA022406
Marketed since
November 5, 2011
Listing expires
December 31, 2026
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Xarelto →

Package NDC codes (1)

Package NDCDescriptionSince
50090-3639-090 TABLET, FILM COATED in 1 BOTTLE (50090-3639-0)Oct 8, 2018

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