Visitor Monitoring Drug History: MEGATOPE
 
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: MEGATOPE
FDA Application No: (NDA) 017837
Active Ingredient(s): ALBUMIN IODINATED I-131 SERUM
Company: ISO TEX
 
Label History
 
Labels are not available on this site for MEGATOPE, (NDA) 017837
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/21/1996 015Control Supplement  
9/30/1985 013Manufacturing Change or Addition  
1/22/1985 012Labeling Revision  
10/4/1983 011Control Supplement  
10/25/1983 010Practioner Draft Labeling  
8/17/1981 009Control Supplement  
11/16/1978 006Labeling Revision  
10/14/1977 005Labeling Revision  
10/14/1977 004Control Supplement  
10/14/1977 003Labeling Revision  
10/14/1977 002Labeling Revision  
10/14/1977 001Labeling Revision  
2/23/1976 000Approval  
 
There are no Therapeutic Equivalents
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