Visitor Monitoring Drug History: METRODIN
 
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: METRODIN
FDA Application No: (NDA) 019415
Active Ingredient(s): UROFOLLITROPIN
Company: SERONO
 
Label History
 
Labels are not available on this site for METRODIN, (NDA) 019415
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/15/2002 030Control Supplement  
12/28/2000 028Control Supplement  
6/19/2000 027Control Supplement  
8/31/2000 026Manufacturing Change or Addition  
7/18/2000 025Control Supplement  
1/21/2000 024Control Supplement  
5/20/1999 023Manufacturing Change or Addition  
4/1/1999 022Control Supplement  
11/24/1999 021Labeling Revision  
4/15/1998 018Manufacturing Change or Addition  
2/18/1998 017Control Supplement  
8/22/1996 016Manufacturing Change or Addition  
1/22/1996 015Manufacturing Change or Addition  
7/12/1995 014Labeling Revision  
8/29/1995 013New Dosage Regimen  
12/6/1993 012Control Supplement  
1/24/1994 011Labeling Revision  
3/28/1994 010Labeling Revision  
8/23/1996 009New Route of Administration  
5/31/1994 008Manufacturing Change or Addition  
1/17/1991 006Control Supplement  
3/14/1990 004Expiration Date Change  
4/25/1988 002Labeling Revision  
3/1/1988 001New or Modified Indication  
9/18/1986 000Approval  
 
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