Visitor Monitoring Drug Details: REPREXAIN
 
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Drug Details

Drug Name: REPREXAIN
FDA Application No: (ANDA) 076642
Active Ingredient(s): HYDROCODONE BITARTRATE; IBUPROFEN
Company: INTERPHARM
Original Approval or Tentative Approval Date: March 18, 2004
 
 
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
HYDROCODONE BITARTRATE AND IBUPROFEN HYDROCODONE BITARTRATE; IBUPROFEN7.5MG; 200MGTABLET; ORAL Prescription No AB
HYDROCODONE BITARTRATE AND IBUPROFEN HYDROCODONE BITARTRATE; IBUPROFEN5MG; 200MGTABLET; ORAL Prescription No AB
REPREXAIN HYDROCODONE BITARTRATE; IBUPROFEN2.5MG; 200MGTABLET; ORAL Prescription No None
REPREXAIN HYDROCODONE BITARTRATE; IBUPROFEN10MG; 200MGTABLET; ORAL Prescription No AB


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