FdaApplication
ANDA 216899
Identifiers
- fda_app_no: ANDA216899
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2024-02-09 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 0.2MG/ML | INJECTABLE;INJECTION |
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 0.5MG/0.5ML | INJECTABLE;INJECTION |
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 1MG/ML | INJECTABLE;INJECTION |
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 2MG/ML | INJECTABLE;INJECTION |
4 products