FdaApplication
ANDA 070679
Identifiers
- fda_app_no: ANDA070679
Properties
| Property | Value |
|---|---|
| applicant_name | QUAD PHARMS |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALOXONE HCL | NALOXONE HYDROCHLORIDE | 0.4MG/ML | Injectable;Injection |
1 product