FdaApplication
ANDA 207108
Identifiers
- fda_app_no: ANDA207108
Properties
| Property | Value |
|---|---|
| applicant_name | PAI HOLDINGS |
| application_type | ANDA |
| approval_date | 2020-04-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 5MG/5ML | SOLUTION;ORAL |
1 product