Visitor Monitoring Drug History: HUMATIN
 
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: HUMATIN
FDA Application No: (ANDA) 062310
Active Ingredient(s): PAROMOMYCIN SULFATE
Company: KING PHARMS
 
Label History
 
Labels are not available on this site for HUMATIN, (ANDA) 062310
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/5/2002 007Facility Addition  
4/5/2002 006Facility Addition  
10/8/1992 002Labeling  
10/8/1992 001Chemistry  
1/5/1981 000Approval  
 
Therapeutic Equivalents
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