VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE)
Summary
FDA approved VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) by ASCENT PHARMS INC. ANDA (Generic) approval (Labeling) on 2023-05-24. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA214419-1
Action Date
2023-05-24
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
VENLAFAXINE HYDROCHLORIDE (generic: VENLAFAXINE), TABLET, EXTENDED RELEASE, ORAL. Application: ANDA214419
Company
Context & Analysis
ASCENT PHARMS INC has 18 FDA actions in our database.
Frequently Asked Questions
How often does ASCENT PHARMS INC have FDA actions?
ASCENT PHARMS INC has 18 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA214419-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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