Visitor Monitoring Drug History: HYDROCORTISONE
 
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Label and Approval History

Drug Name: HYDROCORTISONE
FDA Application No: (ANDA) 074171
Active Ingredient(s): HYDROCORTISONE
Company: TEVA PHARMS
 
Label History
 
Labels are not available on this site for HYDROCORTISONE, (ANDA) 074171
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/9/2002 015Control Supplement  
10/31/2001 014Facility Addition  
10/31/2001 013Facility Addition  
10/31/2001 012Facility Addition  
1/4/2002 011Manufacturing Revision  
1/23/2002 010Facility Addition  
1/4/2002 009Facility Addition  
2/26/2001 008Facility Addition  
2/15/2000 007Manufacturing Revision  
2/15/2000 006Facility Addition  
3/23/1999 004Chemistry  
6/25/1998 003Chemistry  
5/31/1996 002Chemistry  
11/20/1995 001Chemistry  
5/27/1994 000Approval  
 
Therapeutic Equivalents
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