FdaApplication
ANDA 215003
Identifiers
- fda_app_no: ANDA215003
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2021-09-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PAROXETINE HYDROCHLORIDE | PAROXETINE HYDROCHLORIDE | EQ 10MG BASE/5ML | SUSPENSION;ORAL |
1 product