DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
VFEND
FDA Application No:
(NDA) 021464
Active Ingredient(s):
VORICONAZOLE
Company:
PFIZER
Original Approval or Tentative Approval Date:
November 14, 2003
Chemical Type:
6 New indication
Review Classification:
S Standard review drug
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
VFEND
VORICONAZOLE
50MG
Tablet; Oral
Prescription
No
None
VFEND
VORICONAZOLE
200MG
Tablet; Oral
Prescription
No
None
VFEND
VORICONAZOLE
200MG
Injectable; Injection
Prescription
No
None
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