Visitor Monitoring Drug History: NICARDIPINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NICARDIPINE HYDROCHLORIDE
FDA Application No: (ANDA) 074439
Active Ingredient(s): NICARDIPINE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for NICARDIPINE HYDROCHLORIDE, (ANDA) 074439
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/12/2007 014Facility Addition  
7/29/2002 008Facility Addition  
3/12/2002 007Facility Addition  
1/28/2000 006Facility Addition  
11/29/1999 005Facility Addition  
11/26/1999 004Facility Addition  
11/10/1998 003Chemistry  
12/9/1998 002Chemistry  
2/25/1998 001Chemistry  
12/10/1996 000Approval  
 
Therapeutic Equivalents
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