FdaApplication
NDA 017851
Identifiers
- fda_app_no: NDA017851
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1982-01-20 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LIORESAL | BACLOFEN | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| LIORESAL | BACLOFEN | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products