Betaseron - 50419-523-35 - (interferon beta-1b)

Alphabetical Index


Drug Information of Betaseron

Product NDC: 50419-523
Proprietary Name: Betaseron
Non Proprietary Name: interferon beta-1b
Active Ingredient(s):    & nbsp;   interferon beta-1b
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Betaseron

Product NDC: 50419-523
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103471
Marketing Category: BLA
Start Marketing Date: 20090709

Package Information of Betaseron

Package NDC: 50419-523-35
Package Description: 14 TRAY in 1 BOX (50419-523-35) > 1 KIT in 1 TRAY * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE

NDC Information of Betaseron

NDC Code 50419-523-35
Proprietary Name Betaseron
Package Description 14 TRAY in 1 BOX (50419-523-35) > 1 KIT in 1 TRAY * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE
Product NDC 50419-523
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name interferon beta-1b
Dosage Form Name KIT
Route Name
Start Marketing Date 20090709
Marketing Category Name BLA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Betaseron


General Information