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

Drug Name: ACTH
FDA Application No: (NDA) 008317
Active Ingredient(s): CORTICOTROPIN
Company: PARKEDALE
Original Approval or Tentative Approval Date: March 14, 1952
Chemical Type: 5 New manufacturer
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
ACTH CORTICOTROPIN25 UNITS/VIALINJECTABLE; INJECTION Discontinued No None
ACTH CORTICOTROPIN40 UNITS/VIALINJECTABLE; INJECTION Discontinued No None


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