Product NDC: | 45567-0040 |
Proprietary Name: | Kit for the Preparation of Technetium Tc 99m Medronate for Injection |
Non Proprietary Name: | Medronic Acid |
Active Ingredient(s): | 20 mg/10mL & nbsp; Medronic Acid |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45567-0040 |
Labeler Name: | Pharmalucence, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018124 |
Marketing Category: | NDA |
Start Marketing Date: | 19790829 |
Package NDC: | 45567-0040-2 |
Package Description: | 30 VIAL, MULTI-DOSE in 1 KIT (45567-0040-2) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 45567-0040-2 |
Proprietary Name | Kit for the Preparation of Technetium Tc 99m Medronate for Injection |
Package Description | 30 VIAL, MULTI-DOSE in 1 KIT (45567-0040-2) > 10 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 45567-0040 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Medronic Acid |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19790829 |
Marketing Category Name | NDA |
Labeler Name | Pharmalucence, Inc. |
Substance Name | MEDRONIC ACID |
Strength Number | 20 |
Strength Unit | mg/10mL |
Pharmaceutical Classes |