FdaApplication
ANDA 072081
Identifiers
- fda_app_no: ANDA072081
Properties
| Property | Value |
|---|---|
| applicant_name | ASTRAZENECA LP |
| application_type | ANDA |
| approval_date | 1989-04-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALOXONE HYDROCHLORIDE | NALOXONE HYDROCHLORIDE | 0.02MG/ML | INJECTABLE;INJECTION |
1 product