FdaApplication
ANDA 213927
Identifiers
- fda_app_no: ANDA213927
Properties
| Property | Value |
|---|---|
| applicant_name | ADAPTIS PHARMA PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2021-01-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | VENLAFAXINE HYDROCHLORIDE | EQ 75MG BASE | TABLET, EXTENDED RELEASE;ORAL |
1 product