DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(ANDA) 076837
Active Ingredient(s):
FLUCONAZOLE
Company:
TEVA PARENTERAL
Label History
Labels are not available on this site for FLUCONAZOLE IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (ANDA) 076837
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/13/2005
000
Approval
Review
Therapeutic Equivalents
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