Product NDC: | 49609-201 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49609-201 |
Labeler Name: | IBA Molecular North America Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130131 |
Package NDC: | 49609-201-01 |
Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (49609-201-01) |
NDC Code | 49609-201-01 |
Proprietary Name | Ammonia N 13 |
Package Description | 30 mL in 1 VIAL, MULTI-DOSE (49609-201-01) |
Product NDC | 49609-201 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ammonia N-13 |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130131 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | IBA Molecular North America Inc. |
Substance Name | AMMONIA N-13 |
Strength Number | 37.5 |
Strength Unit | mCi/mL |
Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |