FdaApplication
NDA 218343
Identifiers
- fda_app_no: NDA218343
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | NDA |
| approval_date | 2024-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| POTASSIUM PHOSPHATES IN 0.9% SODIUM CHLORIDE | POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC | 1.18GM/250ML (4.72MG/ML);1.12GM/250ML (4.48MG/ML) | SOLUTION;INTRAVENOUS |
1 product