Product NDC: | 23360-151 |
Proprietary Name: | Sterile 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) |
Product NDC: | 23360-151 |
Labeler Name: | Akorn - Strides LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065397 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081231 |
Package NDC: | 23360-151-40 |
Package Description: | 10 VIAL in 1 CARTON (23360-151-40) > 10 mL in 1 VIAL |
NDC Code | 23360-151-40 |
Proprietary Name | Sterile Vancomycin Hydrochloride |
Package Description | 10 VIAL in 1 CARTON (23360-151-40) > 10 mL in 1 VIAL |
Product NDC | 23360-151 |
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 | 20081231 |
Marketing Category Name | ANDA |
Labeler Name | Akorn - Strides LLC |
Substance Name | VANCOMYCIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |