DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BENZYL BENZOATE
FDA Application No:
(ANDA) 084535
Active Ingredient(s):
BENZYL BENZOATE
Company:
LANNETT
Label History
Labels are not available on this site for BENZYL BENZOATE, (ANDA) 084535
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/2/1976
000
Approval
There are no Therapeutic Equivalents
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