Product NDC: | 52670-552 |
Proprietary Name: | Ammonia N 13 |
Non Proprietary Name: | ammonia n-13 |
Active Ingredient(s): | 37.5 mCi/mL & nbsp; ammonia n-13 |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52670-552 |
Labeler Name: | Mayo Clinic |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA203321 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130225 |
Package NDC: | 52670-552-30 |
Package Description: | 30 mL in 1 VIAL, SINGLE-DOSE (52670-552-30) |
NDC Code | 52670-552-30 |
Proprietary Name | Ammonia N 13 |
Package Description | 30 mL in 1 VIAL, SINGLE-DOSE (52670-552-30) |
Product NDC | 52670-552 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ammonia n-13 |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130225 |
Marketing Category Name | ANDA |
Labeler Name | Mayo Clinic |
Substance Name | AMMONIA N-13 |
Strength Number | 37.5 |
Strength Unit | mCi/mL |
Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |