FdaApplication
NDA 020630
Identifiers
- fda_app_no: NDA020630
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN INSTITUTIONAL LLC |
| application_type | NDA |
| approval_date | 1996-07-12 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ULTIVA | REMIFENTANIL HYDROCHLORIDE | EQ 1MG BASE/VIAL | INJECTABLE;INJECTION |
| ULTIVA | REMIFENTANIL HYDROCHLORIDE | EQ 5MG BASE/VIAL | INJECTABLE;INJECTION |
| ULTIVA | REMIFENTANIL HYDROCHLORIDE | EQ 2MG BASE/VIAL | INJECTABLE;INJECTION |
3 products