FdaApplication
NDA 012945
Identifiers
- fda_app_no: NDA012945
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIAMOX | ACETAZOLAMIDE | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
1 product