Home
>
National Drug Code (NDC)
>
Vancomycin Hydrochloride
Vancomycin Hydrochloride - 63323-295-61 - (VANCOMYCIN HYDROCHLORIDE)
Drug Information of Vancomycin Hydrochloride
| Product NDC: | 63323-295 |
| Proprietary Name: | Vancomycin Hydrochloride |
| Non Proprietary Name: | VANCOMYCIN HYDROCHLORIDE |
| Active Ingredient(s): | 5 g/100mL & 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: | 63323-295 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062663 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010717 |
Package Information of Vancomycin Hydrochloride
| Package NDC: | 63323-295-61 |
| Package Description: | 1 BOTTLE in 1 CARTON (63323-295-61) > 100 mL in 1 BOTTLE |
NDC Information of Vancomycin Hydrochloride
| NDC Code | 63323-295-61 |
| Proprietary Name | Vancomycin Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (63323-295-61) > 100 mL in 1 BOTTLE |
| Product NDC | 63323-295 |
| 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 | 20010717 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |
