Visitor Monitoring Drug History: HYTONE
 
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Label and Approval History

Drug Name: HYTONE
FDA Application No: (ANDA) 080472
Active Ingredient(s): HYDROCORTISONE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for HYTONE, (ANDA) 080472
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/27/2002 030Facility Addition  
1/27/1992 028Chemistry  
1/27/1992 027Chemistry  
3/15/1985 025Chemistry  
11/15/1983 021Chemistry  
11/15/1983 020Chemistry  
7/8/1983 018Chemistry  
2/26/1982 017Chemistry  
4/8/1982 016Chemistry  
4/8/1982 015Chemistry  
4/8/1982 006Chemistry  
9/27/1972 000Approval  
 
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