FdaApplication
ANDA 073115
Identifiers
- fda_app_no: ANDA073115
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 1991-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMANTADINE HYDROCHLORIDE | AMANTADINE HYDROCHLORIDE | 50MG/5ML | SYRUP;ORAL |
1 product