Simponi - 57894-070-89 - (golimumab)

Alphabetical Index


Drug Information of Simponi

Product NDC: 57894-070
Proprietary Name: Simponi
Non Proprietary Name: golimumab
Active Ingredient(s): 50    mg/.5mL & nbsp;   golimumab
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Simponi

Product NDC: 57894-070
Labeler Name: Janssen Biotech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125289
Marketing Category: BLA
Start Marketing Date: 20090425

Package Information of Simponi

Package NDC: 57894-070-89
Package Description: 1 SYRINGE in 1 CARTON (57894-070-89) > .5 mL in 1 SYRINGE

NDC Information of Simponi

NDC Code 57894-070-89
Proprietary Name Simponi
Package Description 1 SYRINGE in 1 CARTON (57894-070-89) > .5 mL in 1 SYRINGE
Product NDC 57894-070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name golimumab
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20090425
Marketing Category Name BLA
Labeler Name Janssen Biotech, Inc.
Substance Name GOLIMUMAB
Strength Number 50
Strength Unit mg/.5mL
Pharmaceutical Classes Tumor Necrosis Factor Blocker [EPC]

Complete Information of Simponi


General Information