Visitor Monitoring Drug Details: DIDREX
 
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Drug Details

Drug Name: DIDREX
FDA Application No: (NDA) 012427
Active Ingredient(s): BENZPHETAMINE HYDROCHLORIDE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: October 26, 1960
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
DIDREX BENZPHETAMINE HYDROCHLORIDE50MGTABLET; ORAL Prescription Yes AA
DIDREX BENZPHETAMINE HYDROCHLORIDE25MGTABLET; ORAL Discontinued No None


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