Visitor Monitoring Drug Details: SEMPREX-D
 
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Drug Details

Drug Name: SEMPREX-D
FDA Application No: (NDA) 019806
Active Ingredient(s): ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
Company: UCB INC
Original Approval or Tentative Approval Date: March 25, 1994
Chemical Type: 14 New molecular entity and 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
SEMPREX-D ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE8MG; 60MGCAPSULE; ORAL Prescription Yes None


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