FdaApplication
ANDA 216202
Identifiers
- fda_app_no: ANDA216202
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2022-06-13 |
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