Visitor Monitoring Drug History: CARTEOLOL HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CARTEOLOL HYDROCHLORIDE
FDA Application No: (ANDA) 075476
Active Ingredient(s): CARTEOLOL HYDROCHLORIDE
Company: ALCON
 
Label History
 
Labels are not available on this site for CARTEOLOL HYDROCHLORIDE, (ANDA) 075476
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/23/2002 005Microbiology  
10/1/2002 004Microbiology  
3/22/2002 003Package Change  
5/1/2001 002Packaging Addition  
5/1/2001 001Labeling  
1/3/2000 000Approval Letter
Letter 
8/20/1999 000Tentative Approval Letter
Letter 
 
Therapeutic Equivalents
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