Product NDC: | 45567-0475 |
Proprietary Name: | Kit for the Preparation of Technetium Tc99m Disofenin |
Non Proprietary Name: | HEPATOLITE |
Active Ingredient(s): | 20 mg/10mL & nbsp; HEPATOLITE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45567-0475 |
Labeler Name: | Pharmalucence, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018467 |
Marketing Category: | NDA |
Start Marketing Date: | 19820316 |
Package NDC: | 45567-0475-1 |
Package Description: | 5 VIAL in 1 KIT (45567-0475-1) > 10 mL in 1 VIAL |
NDC Code | 45567-0475-1 |
Proprietary Name | Kit for the Preparation of Technetium Tc99m Disofenin |
Package Description | 5 VIAL in 1 KIT (45567-0475-1) > 10 mL in 1 VIAL |
Product NDC | 45567-0475 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HEPATOLITE |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19820316 |
Marketing Category Name | NDA |
Labeler Name | Pharmalucence, Inc. |
Substance Name | DISOFENIN |
Strength Number | 20 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |