DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TIAGABINE HYDROCHLORIDE
FDA Application No:
(ANDA) 077555
Active Ingredient(s):
TIAGABINE HYDROCHLORIDE
Company:
SUN PHARM INDS LTD
Label History
Labels are not available on this site for TIAGABINE HYDROCHLORIDE, (ANDA) 077555
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/15/2007
000
Tentative Approval
Therapeutic Equivalents
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