FdaApplication
NDA 020298
Identifiers
- fda_app_no: NDA020298
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN INSTITUTIONAL LLC A VIATRIS CO |
| application_type | NDA |
| approval_date | 1996-05-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALOPRIM | ALLOPURINOL SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product