Visitor Monitoring Drug History: THEOPHYLLINE
 
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Label and Approval History

Drug Name: THEOPHYLLINE
FDA Application No: (ANDA) 085863
Active Ingredient(s): THEOPHYLLINE
Company: ACTAVIS MID ATLANTIC
 
Label History
 
Labels are not available on this site for THEOPHYLLINE, (ANDA) 085863
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/23/2000 061Control Supplement  
3/6/1997 059Labeling  
1/14/1997 058Chemistry  
4/4/1996 057Labeling  
7/7/1992 056Labeling  
4/23/1991 055Chemistry in Effect  
9/28/1990 054Chemistry  
3/11/1991 053Chemistry in Effect  
3/28/1990 052Labeling  
10/4/1989 051Labeling  
2/8/1989 049Chemistry  
2/8/1989 048Chemistry  
12/15/1988 047Chemistry  
12/15/1988 046Chemistry  
12/15/1988 045Labeling  
3/17/1987 044Chemistry  
2/18/1983 042Chemistry  
11/21/1970 001Chemistry  
3/16/1979 000Approval  
 
Therapeutic Equivalents
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