| NDC Code | 68083-597-10 | 
|---|
			| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (68083-597-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (68083-597-01) | 
|---|
			| Product NDC | 68083-597 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Vancomycin Hydrochloride | 
|---|
			
			| Non-Proprietary Name | Vancomycin Hydrochloride | 
|---|
			| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 
|---|
			| Usage | INTRAVENOUS | 
|---|
			| Start Marketing Date | 20250321 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA218140 | 
|---|
			| Manufacturer | Gland Pharma Limited | 
|---|
			| Substance Name | VANCOMYCIN HYDROCHLORIDE | 
|---|
			| Strength | 1.5 | 
|---|
			| Strength Unit | g/1 | 
|---|
			| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] | 
|---|