FdaApplication
ANDA 213390
Identifiers
- fda_app_no: ANDA213390
Properties
| Property | Value |
|---|---|
| applicant_name | PROPEL PHARMA CORP |
| application_type | ANDA |
| approval_date | 2021-07-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VIGABATRIN | VIGABATRIN | 500MG/PACKET | FOR SOLUTION;ORAL |
1 product