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Vancomycin Hydrochloride
Vancomycin Hydrochloride - 0781-3188-95 - (Vancomycin Hydrochloride)
Drug Information of Vancomycin Hydrochloride
| Product NDC: | 0781-3188 |
| Proprietary Name: | Vancomycin Hydrochloride |
| Non Proprietary Name: | Vancomycin Hydrochloride |
| Active Ingredient(s): | 1 g/20mL & 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: | 0781-3188 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090250 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100427 |
Package Information of Vancomycin Hydrochloride
| Package NDC: | 0781-3188-95 |
| Package Description: | 10 VIAL in 1 CARTON (0781-3188-95) > 20 mL in 1 VIAL (0781-3188-80) |
NDC Information of Vancomycin Hydrochloride
| NDC Code | 0781-3188-95 |
| Proprietary Name | Vancomycin Hydrochloride |
| Package Description | 10 VIAL in 1 CARTON (0781-3188-95) > 20 mL in 1 VIAL (0781-3188-80) |
| Product NDC | 0781-3188 |
| 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 | 20100427 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |
