Zyvox - 0009-5135-01 - (linezolid)

Alphabetical Index


Drug Information of Zyvox

Product NDC: 0009-5135
Proprietary Name: Zyvox
Non Proprietary Name: linezolid
Active Ingredient(s): 600    mg/1 & nbsp;   linezolid
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Zyvox

Product NDC: 0009-5135
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021130
Marketing Category: NDA
Start Marketing Date: 20000418

Package Information of Zyvox

Package NDC: 0009-5135-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0009-5135-01)

NDC Information of Zyvox

NDC Code 0009-5135-01
Proprietary Name Zyvox
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0009-5135-01)
Product NDC 0009-5135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name linezolid
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000418
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name LINEZOLID
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient]

Complete Information of Zyvox


General Information