FdaApplication
NDA 010721
Identifiers
- fda_app_no: NDA010721
Properties
| Property | Value |
|---|---|
| applicant_name | CASPER PHARMA LLC |
| application_type | NDA |
| approval_date | 1982-01-20 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ANTIVERT | MECLIZINE HYDROCHLORIDE | 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ANTIVERT | MECLIZINE HYDROCHLORIDE | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ANTIVERT | MECLIZINE HYDROCHLORIDE | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| ANTIVERT | MECLIZINE HYDROCHLORIDE | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products