Visitor Monitoring Drug History: ALPHATREX
 
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: ALPHATREX
FDA Application No: (NDA) 019138
Active Ingredient(s): BETAMETHASONE DIPROPIONATE
Company: SAVAGE LABS
 
Label History
 
Labels are not available on this site for ALPHATREX, (NDA) 019138
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/7/1996 011Chemistry  
11/1/1996 010Labeling  
10/31/1988 009Chemistry  
10/31/1988 008Chemistry  
10/31/1988 007Chemistry  
4/23/1987 006Chemistry  
3/18/1986 002Chemistry  
3/28/1986 001Chemistry  
6/26/1984 000Approval  
 
Therapeutic Equivalents
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