Visitor Monitoring Drug Details: TEGRETOL-XR
 
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Drug Details

Drug Name: TEGRETOL-XR
FDA Application No: (NDA) 020234
Active Ingredient(s): CARBAMAZEPINE
Company: NOVARTIS
Original Approval or Tentative Approval Date: March 25, 1996
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TEGRETOL-XR CARBAMAZEPINE100MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
TEGRETOL-XR CARBAMAZEPINE200MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
TEGRETOL-XR CARBAMAZEPINE400MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes None


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