Linezolid - 68462-291-01 - (Linezolid)

Alphabetical Index


Drug Information of Linezolid

Product NDC: 68462-291
Proprietary Name: Linezolid
Non Proprietary Name: Linezolid
Active Ingredient(s): 600    mg/1 & nbsp;   Linezolid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Linezolid

Product NDC: 68462-291
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078987
Marketing Category: ANDA
Start Marketing Date: 20111231

Package Information of Linezolid

Package NDC: 68462-291-01
Package Description: 100 TABLET in 1 BOTTLE (68462-291-01)

NDC Information of Linezolid

NDC Code 68462-291-01
Proprietary Name Linezolid
Package Description 100 TABLET in 1 BOTTLE (68462-291-01)
Product NDC 68462-291
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Linezolid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111231
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name LINEZOLID
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient]

Complete Information of Linezolid


General Information