Product NDC: | 76126-073 |
Proprietary Name: | Vancomycin Hydrochloride |
Non Proprietary Name: | Vancomycin Hydrochloride |
Active Ingredient(s): | 10 g/100mL & nbsp; Vancomycin Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76126-073 |
Labeler Name: | AGILA SPECIALTIES PRIVATE LIMITED |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091554 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110919 |
Package NDC: | 76126-073-01 |
Package Description: | 100 mL in 1 VIAL (76126-073-01) |
NDC Code | 76126-073-01 |
Proprietary Name | Vancomycin Hydrochloride |
Package Description | 100 mL in 1 VIAL (76126-073-01) |
Product NDC | 76126-073 |
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 | 20110919 |
Marketing Category Name | ANDA |
Labeler Name | AGILA SPECIALTIES PRIVATE LIMITED |
Substance Name | VANCOMYCIN HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | g/100mL |
Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |