Composition
- Active ingredients
- VENLAFAXINE HYDROCHLORIDE EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- VENLAFAXINE HYDROCHLORIDE EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA020151-005 · Discontinued
- VENLAFAXINE HYDROCHLORIDE EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA020151-003 · Discontinued
- VENLAFAXINE HYDROCHLORIDE EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA020151-001 · Discontinued
- VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA020151-006 · Discontinued
- VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA020151-004 · Discontinued
- VENLAFAXINE HYDROCHLORIDE EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA020151.
At a glance
- Brand name
- Effexor
- Active substance
- venlafaxine hydrochloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Wyeth Pharms Inc
- Status
- Discontinued
- FDA approval
- 28 Dec 1993
- Application
- NDA020151-002