FdaApplication
NDA 018873
Identifiers
- fda_app_no: NDA018873
Properties
| Property | Value |
|---|---|
| applicant_name | BOEHRINGER INGELHEIM |
| application_type | NDA |
| approval_date | 1985-12-30 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MEXITIL | MEXILETINE HYDROCHLORIDE | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| MEXITIL | MEXILETINE HYDROCHLORIDE | 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| MEXITIL | MEXILETINE HYDROCHLORIDE | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
3 products