Product NDC: | 65857-500 |
Proprietary Name: | Kit for the Preparation of Technetium Tc99m Sestamibi Injection |
Non Proprietary Name: | Kit for the Preparation of Technetium Tc99m Sestamibi Injection |
Active Ingredient(s): | 1 mg/5mL & nbsp; Kit for the Preparation of Technetium Tc99m Sestamibi Injection |
Administration Route(s): | PARENTERAL |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65857-500 |
Labeler Name: | Cardinal Health 414, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078809 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100601 |
Package NDC: | 65857-500-05 |
Package Description: | 5 VIAL in 1 CARTON (65857-500-05) > 5 mL in 1 VIAL |
NDC Code | 65857-500-05 |
Proprietary Name | Kit for the Preparation of Technetium Tc99m Sestamibi Injection |
Package Description | 5 VIAL in 1 CARTON (65857-500-05) > 5 mL in 1 VIAL |
Product NDC | 65857-500 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Kit for the Preparation of Technetium Tc99m Sestamibi Injection |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | PARENTERAL |
Start Marketing Date | 20100601 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health 414, LLC |
Substance Name | TETRAKIS(1-ISOCYANO-2-METHOXY-2-METHYL-PROPANE)-COPPER(I) TETRAFLUOROBORATE |
Strength Number | 1 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |