Visitor Monitoring Drug Details: HALDOL
 
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Drug Details

Drug Name: HALDOL
FDA Application No: (NDA) 015921
Active Ingredient(s): HALOPERIDOL
Company: ORTHO MCNEIL
Original Approval or Tentative Approval Date: April 12, 1967
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
HALDOL HALOPERIDOL0.5MGTABLET; ORAL Discontinued No None
HALDOL HALOPERIDOL1MGTABLET; ORAL Discontinued No None
HALDOL HALOPERIDOL2MGTABLET; ORAL Discontinued No None
HALDOL HALOPERIDOL5MGTABLET; ORAL Discontinued No None
HALDOL HALOPERIDOL10MGTABLET; ORAL Discontinued No None
HALDOL HALOPERIDOL20MGTABLET; ORAL Discontinued No None


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