Visitor Monitoring Drug History: DILTIAZEM HYDROCHLORIDE
 
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Label and Approval History

Drug Name: DILTIAZEM HYDROCHLORIDE
FDA Application No: (ANDA) 074894
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: TEVA PARENTERAL
 
Label History
 
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074894
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/2002 006Expiration Date Change  
4/19/2002 005Package Change  
4/19/2002 004Manufacturing Revision  
4/19/2002 003Control Supplement  
4/19/2002 002Formulation Revision  
4/19/2002 001Labeling  
8/26/1997 000Approval  
 
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