Visitor Monitoring Drug History: THEOCHRON
 
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: THEOCHRON
FDA Application No: (ANDA) 088321
Active Ingredient(s): THEOPHYLLINE
Company: INWOOD LABS
 
Label History
 
Labels are not available on this site for THEOCHRON, (ANDA) 088321
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/28/1998 023Chemistry  
2/7/1997 022Labeling  
7/7/1997 021Chemistry  
7/7/1997 020Chemistry  
10/17/1996 019Labeling  
1/23/1996 018Labeling  
2/22/1993 017Chemistry  
9/3/1991 016SBA  
10/6/1989 015Labeling  
3/24/1989 014Labeling  
1/25/1989 012SBA  
6/20/1988 011Chemistry  
2/9/1988 007Chemistry  
2/9/1988 006Chemistry  
2/9/1988 005Chemistry  
4/29/1986 003Chemistry  
5/11/1987 002Chemistry  
9/19/1985 001Chemistry  
2/21/1985 000Approval  
 
Therapeutic Equivalents
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