EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE)
Summary
FDA approved EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE) by UPJOHN. NDA (New Drug) approval (Labeling) on 2023-08-18. CAPSULE, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA020699-118
Action Date
2023-08-18
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
EFFEXOR XR (generic: VENLAFAXINE HYDROCHLORIDE), CAPSULE, EXTENDED RELEASE, ORAL. Application: NDA020699
Company
Context & Analysis
UPJOHN has 4 FDA actions in our database.
Frequently Asked Questions
How often does UPJOHN have FDA actions?
UPJOHN has 4 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 "NDA020699-118" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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