FdaApplication
ANDA 216364
Identifiers
- fda_app_no: ANDA216364
Properties
| Property | Value |
|---|---|
| applicant_name | OMNIVIUM PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2023-06-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM BICARBONATE | SODIUM BICARBONATE | 50MEQ/50ML (1MEQ/ML) | SOLUTION;INTRAVENOUS |
1 product