Product NDC: | 0019-N120 |
Proprietary Name: | THALLOUS CHLORIDE Tl 201 |
Non Proprietary Name: | thallous chloride, Tl 201 |
Active Ingredient(s): | 1 mCi/mL & nbsp; thallous chloride, Tl 201 |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0019-N120 |
Labeler Name: | Mallinckrodt Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018150 |
Marketing Category: | NDA |
Start Marketing Date: | 20120229 |
Package NDC: | 0019-N120-56 |
Package Description: | 1 VIAL in 1 CAN (0019-N120-56) > 5.6 mL in 1 VIAL |
NDC Code | 0019-N120-56 |
Proprietary Name | THALLOUS CHLORIDE Tl 201 |
Package Description | 1 VIAL in 1 CAN (0019-N120-56) > 5.6 mL in 1 VIAL |
Product NDC | 0019-N120 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | thallous chloride, Tl 201 |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120229 |
Marketing Category Name | NDA |
Labeler Name | Mallinckrodt Inc. |
Substance Name | THALLOUS CHLORIDE TL-201 |
Strength Number | 1 |
Strength Unit | mCi/mL |
Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |