| NDC Code | 51808-210-01 | 
|---|
			| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-210-01) | 
|---|
			| Product NDC | 51808-210 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Dextran 75 | 
|---|
			
			| Non-Proprietary Name | Dextran 75 | 
|---|
			| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 
|---|
			| Usage | INTRAVENOUS | 
|---|
			| Start Marketing Date | 20120701 | 
|---|
			
			| Marketing Category Name | UNAPPROVED DRUG OTHER | 
|---|
			
			| Manufacturer | AnazaoHealth Corporation | 
|---|
			| Substance Name | DEXTRAN 75 | 
|---|
			| Strength | 10 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA] | 
|---|