NDC 50458-579 – Xarelto

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

Human Prescription Drug

Product NDC50458-579

Product details

Brand name
Xarelto
Generic name
Rivaroxaban
Labeler
Janssen Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA022406
Marketed since
November 5, 2011
Listing expires
December 31, 2027
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Xarelto →

Package NDC codes (5)

Package NDCDescriptionSince
50458-579-07 sample7 TABLET, FILM COATED in 1 BOTTLE (50458-579-07)Sep 20, 2016
50458-579-1010 BLISTER PACK in 1 CARTON (50458-579-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (50458-579-01)Nov 5, 2011
50458-579-3030 TABLET, FILM COATED in 1 BOTTLE (50458-579-30)Nov 5, 2011
50458-579-891000 TABLET, FILM COATED in 1 BOTTLE (50458-579-89)Jan 6, 2019
50458-579-9090 TABLET, FILM COATED in 1 BOTTLE (50458-579-90)Nov 5, 2011

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