FdaApplication
ANDA 077781
Identifiers
- fda_app_no: ANDA077781
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC. |
| application_type | ANDA |
| approval_date | 2011-09-27 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GALANTAMINE HYDROBROMIDE | GALANTAMINE HYDROBROMIDE | EQ 4MG BASE | TABLET;ORAL |
| GALANTAMINE HYDROBROMIDE | GALANTAMINE HYDROBROMIDE | EQ 8MG BASE | TABLET;ORAL |
| GALANTAMINE HYDROBROMIDE | GALANTAMINE HYDROBROMIDE | EQ 12MG BASE | TABLET;ORAL |
3 products