| Product NDC: | 67457-220 |
| Proprietary Name: | Isosulfan Blue |
| Non Proprietary Name: | Isosulfan Blue |
| Active Ingredient(s): | 10 mg/mL & nbsp; Isosulfan Blue |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67457-220 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090874 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130314 |
| Package NDC: | 67457-220-05 |
| Package Description: | 6 VIAL, GLASS in 1 CARTON (67457-220-05) > 5 mL in 1 VIAL, GLASS (67457-220-00) |
| NDC Code | 67457-220-05 |
| Proprietary Name | Isosulfan Blue |
| Package Description | 6 VIAL, GLASS in 1 CARTON (67457-220-05) > 5 mL in 1 VIAL, GLASS (67457-220-00) |
| Product NDC | 67457-220 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosulfan Blue |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20130314 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | ISOSULFAN BLUE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |