FdaApplication
NDA 017543
Identifiers
- fda_app_no: NDA017543
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1982-09-30 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUDIOMIL | MAPROTILINE HYDROCHLORIDE | 25MG | TABLET;ORAL |
| LUDIOMIL | MAPROTILINE HYDROCHLORIDE | 75MG | TABLET;ORAL |
| LUDIOMIL | MAPROTILINE HYDROCHLORIDE | 50MG | TABLET;ORAL |
3 products