| Product NDC: | 0019-9091 |
| Proprietary Name: | TechneScan HDP |
| Non Proprietary Name: | Technetium Tc 99m Oxidronate |
| Active Ingredient(s): | 3.15 mg/1 & nbsp; Technetium Tc 99m Oxidronate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0019-9091 |
| Labeler Name: | Mallinckrodt Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018321 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070227 |
| Package NDC: | 0019-9091-40 |
| Package Description: | 30 VIAL in 1 CARTON (0019-9091-40) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
| NDC Code | 0019-9091-40 |
| Proprietary Name | TechneScan HDP |
| Package Description | 30 VIAL in 1 CARTON (0019-9091-40) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
| Product NDC | 0019-9091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Technetium Tc 99m Oxidronate |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20070227 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt Inc. |
| Substance Name | OXIDRONATE DISODIUM |
| Strength Number | 3.15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |