Visitor Monitoring Drug History: PAVULON
 
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: PAVULON
FDA Application No: (NDA) 017015
Active Ingredient(s): PANCURONIUM BROMIDE
Company: ORGANON USA INC
 
Label History
 
Labels are not available on this site for PAVULON, (NDA) 017015
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/22/2000 022Control Supplement  
2/28/1994 021Manufacturing Change or Addition  
5/17/1995 020Control Supplement  
10/5/1990 019Manufacturing Change or Addition  
7/25/1991 018Labeling Revision  
3/29/1993 016Expiration Date Change  
10/8/1987 013Control Supplement  
6/27/1986 011Control Supplement  
4/2/1986 010Practioner Draft Labeling  
3/17/1982 009Labeling Revision  
3/17/1982 008Manufacturing Change or Addition  
1/26/1977 007Expiration Date Change  
9/22/1975 006Labeling Revision  
10/8/1974 005Control Supplement  
11/11/1974 003Final Printed Labeling - MarkIV  
10/24/1972 000Approval  
 
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