| 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 |