Visitor Monitoring Drug History: LARGON
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: LARGON
FDA Application No: (NDA) 012382
Active Ingredient(s): PROPIOMAZINE HYDROCHLORIDE
Company: BAXTER HLTHCARE CORP
 
Label History
 
Labels are not available on this site for LARGON, (NDA) 012382
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/5/1994 013Control Supplement  
12/5/1960 000Approval  
 
There are no Therapeutic Equivalents
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