Product NDC: | 55154-3938 |
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) |
Product NDC: | 55154-3938 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021130 |
Marketing Category: | NDA |
Start Marketing Date: | 20000418 |
Package NDC: | 55154-3938-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-3938-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 55154-3938-0 |
Proprietary Name | Zyvox |
Package Description | 10 BLISTER PACK in 1 BAG (55154-3938-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 55154-3938 |
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 | Cardinal Health |
Substance Name | LINEZOLID |
Strength Number | 600 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient] |