FdaApplication
ANDA 071672
Identifiers
- fda_app_no: ANDA071672
Properties
| Property | Value |
|---|---|
| applicant_name | SOLOPAK MEDICAL PRODUCTS INC |
| application_type | ANDA |
| approval_date | 1987-11-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALOXONE HYDROCHLORIDE | NALOXONE HYDROCHLORIDE | 0.02MG/ML | INJECTABLE;INJECTION |
1 product