FdaApplication
NDA 011721
Identifiers
- fda_app_no: NDA011721
Properties
| Property | Value |
|---|---|
| applicant_name | LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO |
| application_type | NDA |
| approval_date | 1991-11-25 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEPTAZANE | METHAZOLAMIDE | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| NEPTAZANE | METHAZOLAMIDE | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products