FdaApplication
ANDA 219917
Identifiers
- fda_app_no: ANDA219917
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2025-10-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LOFEXIDINE HYDROCHLORIDE | LOFEXIDINE HYDROCHLORIDE | EQ 0.18MG BASE | TABLET;ORAL |
1 product