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 |