Visitor Monitoring Drug History: ANECTINE
 
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: ANECTINE
FDA Application No: (NDA) 008453
Active Ingredient(s): SUCCINYLCHOLINE CHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for ANECTINE, (NDA) 008453
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/2/2000 019Labeling Revision  
4/10/1997 018Manufacturing Change or Addition  
11/28/1994 017Labeling Revision  
9/26/2000 016Labeling Revision  
10/29/1993 015Labeling Revision  
11/10/1987 014Labeling Revision  
5/1/1985 013Labeling Revision  
2/11/1982 012Package Change Review 
5/15/1981 011Control Supplement  
2/12/1981 010Control Supplement  
12/22/1981 009Labeling Revision  
11/21/1980 008Control Supplement  
5/22/1985 007Formulation Revision  
3/30/1978 006Control Supplement Review 
12/5/1975 004Labeling Revision Review 
6/22/1973 001Final Printed Labeling - MarkIV Review 
8/20/1952 000Approval  
 
There are no Therapeutic Equivalents
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