Visitor Monitoring Drug Details: ALPRAZOLAM
 
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Drug Details

Drug Name: ALPRAZOLAM
FDA Application No: (ANDA) 077979
Active Ingredient(s): ALPRAZOLAM
Company: TEVA PHARMS
Original Approval or Tentative Approval Date: February 28, 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
ALPRAZOLAM ALPRAZOLAM0.5MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
ALPRAZOLAM ALPRAZOLAM1MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
ALPRAZOLAM ALPRAZOLAM2MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
ALPRAZOLAM ALPRAZOLAM3MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB


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