| NDC Code | 70511-102-20 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (70511-102-20) / 20 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 70511-102 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Sodium Phenylacetate And Sodium Benzoate |
|---|
| Non-Proprietary Name | Sodium Phenylacetate And Sodium Benzoate |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20210701 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA215025 |
|---|
| Manufacturer | MAIA PHARMACEUTICALS |
|---|
| Substance Name | SODIUM BENZOATE; SODIUM PHENYLACETATE |
|---|
| Strength | 100; 100 |
|---|
| Strength Unit | mg/mL; mg/mL |
|---|
| Pharmacy Classes | Ammonium Ion Binding Activity [MoA], Ammonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC], Nitrogen Binding Agent [EPC] |
|---|