Visitor Monitoring Drug History: FASTIN
 
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: FASTIN
FDA Application No: (NDA) 017352
Active Ingredient(s): PHENTERMINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for FASTIN, (NDA) 017352
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/16/1998 019Labeling Revision  
1/16/1998 018Labeling Revision  
10/10/1997 017Labeling Revision  
4/24/1989 014Manufacturing Change or Addition  
7/31/1984 011Package Change  
8/31/1981 010Expiration Date Change  
8/31/1981 009Manufacturing Change or Addition  
7/17/1981 008Manufacturing Change or Addition  
9/26/1980 007Control Supplement  
7/29/1980 006Labeling Revision  
10/11/1978 005Expiration Date Change  
2/2/1977 004Control Supplement  
7/22/1975 003Control Supplement  
12/3/1975 002Control Supplement  
4/10/1975 001Control Supplement  
8/14/1973 000Approval  
 
Therapeutic Equivalents
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