Visitor Monitoring Drug History: NICARDIPINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NICARDIPINE HYDROCHLORIDE
FDA Application No: (ANDA) 074540
Active Ingredient(s): NICARDIPINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for NICARDIPINE HYDROCHLORIDE, (ANDA) 074540
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/5/2001 011Labeling  
8/30/2001 010Facility Addition  
2/25/2000 009Labeling  
7/7/2000 008Facility Addition  
10/29/1999 007Manufacturing Revision  
10/29/1999 006Control Supplement  
3/9/1998 004Chemistry  
7/11/1997 003Chemistry  
7/11/1997 002Chemistry  
7/11/1997 001Chemistry  
10/28/1996 000Approval  
 
Therapeutic Equivalents
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