Visitor Monitoring Drug History: FLUOTHANE
 
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: FLUOTHANE
FDA Application No: (NDA) 011338
Active Ingredient(s): HALOTHANE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for FLUOTHANE, (NDA) 011338
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/29/1996 018Expiration Date Change  
4/29/1996 017Package Change  
2/28/1994 016Manufacturing Change or Addition  
7/30/1987 015Labeling Revision  
7/30/1987 014Expiration Date Change  
10/1/1982 013Control Supplement  
12/3/1981 011Control Supplement  
12/1/1981 009Labeling Revision  
12/1/1981 008Control Supplement  
12/4/1979 007Labeling Revision  
10/23/1978 006Labeling Revision  
10/28/1975 005Labeling Revision  
10/28/1975 004Control Supplement  
3/12/1958 000Approval  
 
Therapeutic Equivalents
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