FdaApplication
NDA 019500
Identifiers
- fda_app_no: NDA019500
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1986-12-15 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LAMPRENE | CLOFAZIMINE | 50MG | CAPSULE;ORAL |
| LAMPRENE | CLOFAZIMINE | 100MG | CAPSULE;ORAL |
2 products