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VANCOMYCIN HYDROCHLORIDE
VANCOMYCIN HYDROCHLORIDE - 0338-3580-48 - (VANCOMYCIN HYDROCHLORIDE)
Drug Information of VANCOMYCIN HYDROCHLORIDE
| Product NDC: | 0338-3580 |
| Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Non Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Active Ingredient(s): | 750 mg/150mL & nbsp; VANCOMYCIN HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VANCOMYCIN HYDROCHLORIDE
| Product NDC: | 0338-3580 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050671 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120117 |
Package Information of VANCOMYCIN HYDROCHLORIDE
| Package NDC: | 0338-3580-48 |
| Package Description: | 200 mL in 1 BAG (0338-3580-48) |
NDC Information of VANCOMYCIN HYDROCHLORIDE
| NDC Code | 0338-3580-48 |
| Proprietary Name | VANCOMYCIN HYDROCHLORIDE |
| Package Description | 200 mL in 1 BAG (0338-3580-48) |
| Product NDC | 0338-3580 |
| 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 | 750 |
| Strength Unit | mg/150mL |
| Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |
