Visitor Monitoring Drug Details: TENUATE
 
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Drug Details

Drug Name: TENUATE
FDA Application No: (NDA) 011722
Active Ingredient(s): DIETHYLPROPION HYDROCHLORIDE
Company: WATSON PHARMS
Original Approval or Tentative Approval Date: August 6, 1959
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TENUATE DIETHYLPROPION HYDROCHLORIDE25MGTABLET; ORAL Prescription Yes None


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