Visitor Monitoring Drug Details: GABITRIL
 
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Drug Details

Drug Name: GABITRIL
FDA Application No: (NDA) 020646
Active Ingredient(s): TIAGABINE HYDROCHLORIDE
Company: CEPHALON
Original Approval or Tentative Approval Date: September 30, 1997
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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
GABITRIL TIAGABINE HYDROCHLORIDE4MGTABLET; ORAL Prescription No None
GABITRIL TIAGABINE HYDROCHLORIDE12MGTABLET; ORAL Prescription No None
GABITRIL TIAGABINE HYDROCHLORIDE16MGTABLET; ORAL Prescription Yes None
GABITRIL TIAGABINE HYDROCHLORIDE20MGTABLET; ORAL Discontinued No None
GABITRIL TIAGABINE HYDROCHLORIDE2MGTABLET; ORAL Prescription Yes None
GABITRIL TIAGABINE HYDROCHLORIDE6MGTABLET; ORAL Prescription No None
GABITRIL TIAGABINE HYDROCHLORIDE8MGTABLET; ORAL Prescription No None
GABITRIL TIAGABINE HYDROCHLORIDE10MGTABLET; ORAL Prescription No None


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