Zyvox - 0009-5139-01 - (linezolid)

Alphabetical Index


Drug Information of Zyvox

Product NDC: 0009-5139
Proprietary Name: Zyvox
Non Proprietary Name: linezolid
Active Ingredient(s): 400    mg/200mL & nbsp;   linezolid
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zyvox

Product NDC: 0009-5139
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021131
Marketing Category: NDA
Start Marketing Date: 20000418

Package Information of Zyvox

Package NDC: 0009-5139-01
Package Description: 200 mL in 1 BAG (0009-5139-01)

NDC Information of Zyvox

NDC Code 0009-5139-01
Proprietary Name Zyvox
Package Description 200 mL in 1 BAG (0009-5139-01)
Product NDC 0009-5139
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name linezolid
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20000418
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name LINEZOLID
Strength Number 400
Strength Unit mg/200mL
Pharmaceutical Classes Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient]

Complete Information of Zyvox


General Information