FdaApplication
NDA 019879
Identifiers
- fda_app_no: NDA019879
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1990-11-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ORNIDYL | EFLORNITHINE HYDROCHLORIDE | 200MG/ML | INJECTABLE;INJECTION |
1 product