DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
EFFEXOR XR
FDA Application No:
(NDA) 020699
Active Ingredient(s):
VENLAFAXINE HYDROCHLORIDE
Company:
WYETH PHARMS INC
Original Approval or Tentative Approval Date:
October 20, 1997
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
EFFEXOR XR
VENLAFAXINE HYDROCHLORIDE
EQ 37.5MG BASE
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
None
EFFEXOR XR
VENLAFAXINE HYDROCHLORIDE
EQ 75MG BASE
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
None
EFFEXOR XR
VENLAFAXINE HYDROCHLORIDE
EQ 100MG BASE
CAPSULE, EXTENDED RELEASE; ORAL
Discontinued
No
None
EFFEXOR XR
VENLAFAXINE HYDROCHLORIDE
EQ 150MG BASE
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
Yes
None
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