Visitor Monitoring Drug Details: SEPTRA DS
 
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Drug Details

Drug Name: SEPTRA DS
FDA Application No: (NDA) 017376
Active Ingredient(s): SULFAMETHOXAZOLE; TRIMETHOPRIM
Company: MONARCH PHARMS
Original Approval or Tentative Approval Date: July 30, 1973
Chemical Type: 14 New molecular entity and new combination
Review Classification: P Priority review drug
 
There are no Therapeutic Equivalents Label Information
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
SEPTRA SULFAMETHOXAZOLE; TRIMETHOPRIM400MG; 80MGTABLET; ORAL Prescription No AB
SEPTRA DS SULFAMETHOXAZOLE; TRIMETHOPRIM800MG; 160MGTABLET; ORAL Prescription No AB


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