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VANCOMYCIN HYDROCHLORIDE
VANCOMYCIN HYDROCHLORIDE - 63323-221-10 - (VANCOMYCIN HYDROCHLORIDE)
Drug Information of VANCOMYCIN HYDROCHLORIDE
| Product NDC: | 63323-221 |
| Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Non Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Active Ingredient(s): | 500 mg/10mL & 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: | 63323-221 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062663 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000901 |
Package Information of VANCOMYCIN HYDROCHLORIDE
| Package NDC: | 63323-221-10 |
| Package Description: | 25 VIAL in 1 TRAY (63323-221-10) > 10 mL in 1 VIAL |
NDC Information of VANCOMYCIN HYDROCHLORIDE
| NDC Code | 63323-221-10 |
| Proprietary Name | VANCOMYCIN HYDROCHLORIDE |
| Package Description | 25 VIAL in 1 TRAY (63323-221-10) > 10 mL in 1 VIAL |
| Product NDC | 63323-221 |
| 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 | 20000901 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |
