FdaApplication
NDA 220790
Identifiers
- fda_app_no: NDA220790
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | NDA |
| approval_date | 2026-07-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM BICARBONATE | SODIUM BICARBONATE | 150MEQ/1000ML (0.15MEQ/ML) | SOLUTION;INTRAVENOUS |
1 product