Visitor Monitoring Drug Details: LACTULOSE
 
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Drug Details

Drug Name: LACTULOSE
FDA Application No: (ANDA) 074712
Active Ingredient(s): LACTULOSE
Company: INALCO
Original Approval or Tentative Approval Date: December 10, 1997
 
There are no 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
LACTULOSE LACTULOSE10GM/PACKETFOR SOLUTION; ORAL Prescription Yes None
LACTULOSE LACTULOSE20GM/PACKETFOR SOLUTION; ORAL Prescription Yes None


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