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Zyvox
Zyvox - 49349-751-18 - (linezolid)
Drug Information of Zyvox
| Product NDC: | 49349-751 |
| 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: | 49349-751 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021130 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130403 |
Package Information of Zyvox
| Package NDC: | 49349-751-18 |
| Package Description: | 18 TABLET, FILM COATED in 1 VIAL (49349-751-18) |
NDC Information of Zyvox
| NDC Code | 49349-751-18 |
| Proprietary Name | Zyvox |
| Package Description | 18 TABLET, FILM COATED in 1 VIAL (49349-751-18) |
| Product NDC | 49349-751 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | linezolid |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130403 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LINEZOLID |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient] |
