Visitor Monitoring Drug History: MEPERIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: MEPERIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 088639
Active Ingredient(s): MEPERIDINE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for MEPERIDINE HYDROCHLORIDE, (ANDA) 088639
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/27/2001 026Manufacturing Revision  
7/27/2001 025Facility Addition  
10/30/2000 023Control Supplement  
12/21/1999 022Facility Addition  
5/20/1999 021Chemistry  
3/12/1999 020Chemistry  
12/1/1998 019Chemistry  
1/24/1997 018Chemistry  
1/24/1997 017Chemistry  
1/24/1997 016Chemistry  
1/24/1997 015Chemistry  
12/23/1994 014Chemistry  
3/2/1994 013Labeling  
4/3/1992 012Chemistry  
4/3/1992 010Chemistry  
7/30/1991 009Labeling  
10/27/1989 008Labeling  
10/10/1989 007Labeling  
1/3/1990 005Chemistry  
4/30/1985 003Chemistry  
7/2/1984 000Approval  
 
Therapeutic Equivalents
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