NDC 50458-580 – Xarelto

Rivaroxaban 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50458-580

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
July 1, 2011
Listing expires
December 31, 2027
Pharmacologic class
Factor Xa Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Xarelto →

Package NDC codes (4)

Package NDCDescriptionSince
50458-580-07 sample7 TABLET, FILM COATED in 1 BOTTLE (50458-580-07)Nov 1, 2017
50458-580-1010 BLISTER PACK in 1 CARTON (50458-580-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (50458-580-01)Jul 1, 2011
50458-580-3030 TABLET, FILM COATED in 1 BOTTLE (50458-580-30)Jul 1, 2011
50458-580-9090 TABLET, FILM COATED in 1 BOTTLE (50458-580-90)Nov 1, 2017

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