FdaApplication
NDA 020031
Identifiers
- fda_app_no: NDA020031
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | NDA |
| approval_date | 1992-12-29 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PAXIL | PAROXETINE HYDROCHLORIDE | EQ 10MG BASE | TABLET;ORAL |
| PAXIL | PAROXETINE HYDROCHLORIDE | EQ 40MG BASE | TABLET;ORAL |
| PAXIL | PAROXETINE HYDROCHLORIDE | EQ 20MG BASE | TABLET;ORAL |
| PAXIL | PAROXETINE HYDROCHLORIDE | EQ 50MG BASE | TABLET;ORAL |
| PAXIL | PAROXETINE HYDROCHLORIDE | EQ 30MG BASE | TABLET;ORAL |
5 products