FdaApplication
ANDA 217561
Identifiers
- fda_app_no: ANDA217561
Properties
| Property | Value |
|---|---|
| applicant_name | NEXUS PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2024-11-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLENE BLUE | METHYLENE BLUE | 50MG/10ML (5MG/ML) | SOLUTION;INTRAVENOUS |
1 product