Visitor Monitoring Drug Details: CYLERT
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: CYLERT
FDA Application No: (NDA) 016832
Active Ingredient(s): PEMOLINE
Company: ABBOTT
Original Approval or Tentative Approval Date: January 27, 1975
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
CYLERT PEMOLINE18.75MGTABLET; ORAL Discontinued No None
CYLERT PEMOLINE37.5MGTABLET; ORAL Discontinued No None
CYLERT PEMOLINE75MGTABLET; ORAL Discontinued No None


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