FdaApplication
ANDA 074317
Identifiers
- fda_app_no: ANDA074317
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1995-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 10MG/ML | INJECTABLE;INJECTION |
1 product