FdaApplication
NDA 019034
Identifiers
- fda_app_no: NDA019034
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 1984-01-11 |
Products (7)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 2MG/ML | INJECTABLE;INJECTION |
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 4MG/ML | INJECTABLE;INJECTION |
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 0.5MG/0.5ML | INJECTABLE;INJECTION |
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 0.2MG/ML | INJECTABLE;INJECTION |
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1MG/ML | INJECTABLE;INJECTION |
| DILAUDID-HP | HYDROMORPHONE HYDROCHLORIDE | 250MG/VIAL | INJECTABLE;INJECTION |
| DILAUDID-HP | HYDROMORPHONE HYDROCHLORIDE | 10MG/ML | INJECTABLE;INJECTION |
7 products