Visitor Monitoring Drug History: OCTREOTIDE ACETATE
 
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Label and Approval History

Drug Name: OCTREOTIDE ACETATE
FDA Application No: (ANDA) 077372
Active Ingredient(s): OCTREOTIDE ACETATE
Company: SUN PHARM INDS
 
Label History
 
Labels are not available on this site for OCTREOTIDE ACETATE, (ANDA) 077372
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/14/2007 000Approval  
 
Therapeutic Equivalents
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