FdaApplication
ANDA 214211
Identifiers
- fda_app_no: ANDA214211
Properties
| Property | Value |
|---|---|
| applicant_name | STERINOVA INC |
| application_type | ANDA |
| approval_date | 2025-08-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALOXONE HYDROCHLORIDE | NALOXONE HYDROCHLORIDE | 0.4MG/ML | INJECTABLE;INJECTION |
1 product