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

Drug Name: LEVATOL
FDA Application No: (NDA) 018976
Active Ingredient(s): PENBUTOLOL SULFATE
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: December 30, 1987
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no 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
LEVATOL PENBUTOLOL SULFATE10MGTABLET; ORAL Discontinued No None
LEVATOL PENBUTOLOL SULFATE20MGTABLET; ORAL Prescription Yes None


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