FdaApplication
NDA 019891
Identifiers
- fda_app_no: NDA019891
Properties
| Property | Value |
|---|---|
| applicant_name | RHODES PHARMACEUTICALS LP |
| application_type | NDA |
| approval_date | 1992-12-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 5MG/5ML | SOLUTION;ORAL |
1 product