Product NDC: | 0019-9132 |
Proprietary Name: | INDIUM IN 111 CHLORIDE |
Non Proprietary Name: | indium in 111 chloride |
Active Ingredient(s): | 10 mCi/mL & nbsp; indium in 111 chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0019-9132 |
Labeler Name: | Mallinckrodt Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019841 |
Marketing Category: | NDA |
Start Marketing Date: | 20071207 |
Package NDC: | 0019-9132-06 |
Package Description: | 1 VIAL, GLASS in 1 CAN (0019-9132-06) > .5 mL in 1 VIAL, GLASS |
NDC Code | 0019-9132-06 |
Proprietary Name | INDIUM IN 111 CHLORIDE |
Package Description | 1 VIAL, GLASS in 1 CAN (0019-9132-06) > .5 mL in 1 VIAL, GLASS |
Product NDC | 0019-9132 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | indium in 111 chloride |
Dosage Form Name | SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20071207 |
Marketing Category Name | NDA |
Labeler Name | Mallinckrodt Inc. |
Substance Name | INDIUM IN-111 CHLORIDE |
Strength Number | 10 |
Strength Unit | mCi/mL |
Pharmaceutical Classes |