FdaApplication
ANDA 218912
Identifiers
- fda_app_no: ANDA218912
Properties
| Property | Value |
|---|---|
| applicant_name | LEADING PHARMA LLC |
| application_type | ANDA |
| approval_date | 2024-09-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCHLORPERAZINE MALEATE | PROCHLORPERAZINE MALEATE | EQ 5MG BASE | TABLET;ORAL |
| PROCHLORPERAZINE MALEATE | PROCHLORPERAZINE MALEATE | EQ 10MG BASE | TABLET;ORAL |
2 products