Visitor Monitoring Drug Details: ULTRACET
 
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Drug Details

Drug Name: ULTRACET
FDA Application No: (NDA) 021123
Active Ingredient(s): ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Company: ORTHO MCNEIL PHARM
Original Approval or Tentative Approval Date: August 15, 2001
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
 
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
ULTRACET ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE325MG; 37.5MGTABLET; ORAL Prescription Yes AB


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