Xarelto - 50458-579-99 - (rivaroxaban)

Alphabetical Index


Drug Information of Xarelto

Product NDC: 50458-579
Proprietary Name: Xarelto
Non Proprietary Name: rivaroxaban
Active Ingredient(s): 20    mg/1 & nbsp;   rivaroxaban
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Xarelto

Product NDC: 50458-579
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202439
Marketing Category: NDA
Start Marketing Date: 20111105

Package Information of Xarelto

Package NDC: 50458-579-99
Package Description: 1 BOTTLE in 1 CARTON (50458-579-99) > 5 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Xarelto

NDC Code 50458-579-99
Proprietary Name Xarelto
Package Description 1 BOTTLE in 1 CARTON (50458-579-99) > 5 TABLET, FILM COATED in 1 BOTTLE
Product NDC 50458-579
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rivaroxaban
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111105
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name RIVAROXABAN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Factor Xa Inhibitors [MoA],Factor Xa Inhibitor [EPC]

Complete Information of Xarelto


General Information