| 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: | 45567-0040-1 |
| Package Description: | 5 VIAL, MULTI-DOSE in 1 KIT (45567-0040-1) > 10 mL in 1 VIAL, MULTI-DOSE |
| NDC Code | 45567-0040-1 |
| Proprietary Name | Kit for the Preparation of Technetium Tc 99m Medronate for Injection |
| Package Description | 5 VIAL, MULTI-DOSE in 1 KIT (45567-0040-1) > 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 |