Visitor Monitoring Drug Details: GABAPENTIN
 
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Drug Details

Drug Name: GABAPENTIN
FDA Application No: (ANDA) 077242
Active Ingredient(s): GABAPENTIN
Company: SUN PHARM INDS LTD
Original Approval or Tentative Approval Date: August 24, 2006
 
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
GABAPENTIN GABAPENTIN100MGCAPSULE; ORAL Prescription No AB
GABAPENTIN GABAPENTIN300MGCAPSULE; ORAL Prescription No AB
GABAPENTIN GABAPENTIN400MGCAPSULE; ORAL Prescription No AB


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