Visitor Monitoring Drug Details: TIAGABINE HYDROCHLORIDE
 
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Drug Details

Drug Name: TIAGABINE HYDROCHLORIDE
FDA Application No: (ANDA) 077555
Active Ingredient(s): TIAGABINE HYDROCHLORIDE
Company: SUN PHARM INDS LTD
Original Approval or Tentative Approval Date: March 15, 2007
 
Therapeutic Equivalents Labels are not available
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 NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TIAGABINE HYDROCHLORIDE TIAGABINE HYDROCHLORIDE2MGTABLET; ORAL Tentative Approval No None
TIAGABINE HYDROCHLORIDE TIAGABINE HYDROCHLORIDE4MGTABLET; ORAL Tentative Approval No None


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