Visitor Monitoring Drug History: FACTREL
 
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: FACTREL
FDA Application No: (NDA) 018123
Active Ingredient(s): GONADORELIN HYDROCHLORIDE
Company: BAXTER HLTHCARE CORP
 
Label History
 
Labels are not available on this site for FACTREL, (NDA) 018123
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/19/2002 014Control Supplement Letter 
6/2/2000 012Expiration Date Change  
5/9/1994 011Labeling Revision  
2/22/1994 010Labeling Revision  
7/30/1990 009Labeling Revision  
11/8/1989 008Labeling Revision  
8/8/1989 007Labeling Revision  
11/21/1989 006Package Change  
7/27/1989 005Control Supplement  
2/24/1988 004Control Supplement  
5/29/1987 002Labeling Revision  
5/19/1983 001Labeling Revision  
9/30/1982 000Approval  
 
There are no Therapeutic Equivalents
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