FdaApplication
ANDA 200143
Identifiers
- fda_app_no: ANDA200143
Properties
| Property | Value |
|---|---|
| applicant_name | BARR LABORATORIES INC SUB TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 2013-11-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACAMPROSATE CALCIUM | ACAMPROSATE CALCIUM | 333MG | TABLET, DELAYED RELEASE;ORAL |
1 product