Visitor Monitoring Drug History: RENOQUID
 
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: RENOQUID
FDA Application No: (NDA) 017569
Active Ingredient(s): SULFACYTINE
Company: GLENWOOD
 
Label History
 
Labels are not available on this site for RENOQUID, (NDA) 017569
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/16/1986 006Practioner Draft Labeling  
4/9/1981 005Manufacturing Change or Addition  
10/23/1979 004Manufacturing Change or Addition  
7/5/1978 003Manufacturing Change or Addition  
1/12/1978 002Expiration Date Change  
11/22/1976 001Package Change  
9/12/1975 000Approval  
 
There are no Therapeutic Equivalents
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