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Dextran 75
Dextran 75 - 51808-210-01 - (Dextran 75)
Drug Information of Dextran 75
| Product NDC: | 51808-210 |
| Proprietary Name: | Dextran 75 |
| Non Proprietary Name: | Dextran 75 |
| Active Ingredient(s): | 10 mg/1 & nbsp; Dextran 75 |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextran 75
| Product NDC: | 51808-210 |
| Labeler Name: | AnazaoHealth Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120701 |
Package Information of Dextran 75
| Package NDC: | 51808-210-01 |
| Package Description: | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-210-01) |
NDC Information of Dextran 75
| NDC Code | 51808-210-01 |
| Proprietary Name | Dextran 75 |
| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-210-01) |
| Product NDC | 51808-210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dextran 75 |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120701 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AnazaoHealth Corporation |
| Substance Name | DEXTRAN 75 |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA] |
