FdaApplication
ANDA 070190
Identifiers
- fda_app_no: ANDA070190
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH AYERST LABORATORIES |
| application_type | ANDA |
| approval_date | 1986-09-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALOXONE | NALOXONE HYDROCHLORIDE | 0.4MG/ML | INJECTABLE;INJECTION |
1 product