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Ammonul
Ammonul - 62592-720-50 - (sodium phenylacetate and sodium benzoate)
Drug Information of Ammonul
| Product NDC: | 62592-720 |
| Proprietary Name: | Ammonul |
| Non Proprietary Name: | sodium phenylacetate and sodium benzoate |
| Active Ingredient(s): | 100; 100 mg/mL; mg/mL & nbsp; sodium phenylacetate and sodium benzoate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ammonul
| Product NDC: | 62592-720 |
| Labeler Name: | Ucyclyd Pharma Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020645 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050217 |
Package Information of Ammonul
| Package NDC: | 62592-720-50 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (62592-720-50) > 50 mL in 1 VIAL, SINGLE-USE |
NDC Information of Ammonul
| NDC Code | 62592-720-50 |
| Proprietary Name | Ammonul |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (62592-720-50) > 50 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 62592-720 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium phenylacetate and sodium benzoate |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050217 |
| Marketing Category Name | NDA |
| Labeler Name | Ucyclyd Pharma Inc. |
| Substance Name | SODIUM BENZOATE; SODIUM PHENYLACETATE |
| Strength Number | 100; 100 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC],Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC] |
