DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FEXOFENADINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076502
Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for FEXOFENADINE HYDROCHLORIDE, (ANDA) 076502
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/12/2006
000
Approval
Therapeutic Equivalents
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