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: | 0019-9091-20 |
Package Description: | 5 VIAL in 1 CELLO PACK (0019-9091-20) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
NDC Code | 0019-9091-20 |
Proprietary Name | TechneScan HDP |
Package Description | 5 VIAL in 1 CELLO PACK (0019-9091-20) > 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 |