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Vancomycin Hydrochloride
Vancomycin Hydrochloride - 0409-6531-02 - (VANCOMYCIN HYDROCHLORIDE)
Drug Information of Vancomycin Hydrochloride
| Product NDC: | 0409-6531 |
| Proprietary Name: | Vancomycin Hydrochloride |
| Non Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Active Ingredient(s): | 750 mg/15mL & nbsp; VANCOMYCIN HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vancomycin Hydrochloride
| Product NDC: | 0409-6531 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062912 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880804 |
Package Information of Vancomycin Hydrochloride
| Package NDC: | 0409-6531-02 |
| Package Description: | 10 VIAL in 1 TRAY (0409-6531-02) > 15 mL in 1 VIAL |
NDC Information of Vancomycin Hydrochloride
| NDC Code | 0409-6531-02 |
| Proprietary Name | Vancomycin Hydrochloride |
| Package Description | 10 VIAL in 1 TRAY (0409-6531-02) > 15 mL in 1 VIAL |
| Product NDC | 0409-6531 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VANCOMYCIN HYDROCHLORIDE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19880804 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |
