Visitor Monitoring Drug History: ASTRAMORPH PF
 
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Label and Approval History

Drug Name: ASTRAMORPH PF
FDA Application No: (ANDA) 071052
Active Ingredient(s): MORPHINE SULFATE
Company: ABRAXIS BIOSCIENCE
 
Label History
 
Labels are not available on this site for ASTRAMORPH PF, (ANDA) 071052
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/2/2002 009Labeling  
12/22/1997 007Chemistry  
5/31/1996 006Chemistry  
8/25/1995 005Chemistry  
12/16/1988 003Labeling  
12/16/1988 002Chemistry  
12/16/1988 001Chemistry  
10/7/1986 000Approval  
 
Therapeutic Equivalents
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