Product NDC: | 0338-3552 |
Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
Non Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
Active Ingredient(s): | 1 g/200mL & nbsp; VANCOMYCIN HYDROCHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-3552 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050671 |
Marketing Category: | NDA |
Start Marketing Date: | 20120117 |
Package NDC: | 0338-3552-48 |
Package Description: | 200 mL in 1 BAG (0338-3552-48) |
NDC Code | 0338-3552-48 |
Proprietary Name | VANCOMYCIN HYDROCHLORIDE |
Package Description | 200 mL in 1 BAG (0338-3552-48) |
Product NDC | 0338-3552 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | VANCOMYCIN HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120117 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | VANCOMYCIN HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | g/200mL |
Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |