Visitor Monitoring Drug History: GALANTAMINE HYDROBROMIDE
 
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Label and Approval History

Drug Name: GALANTAMINE HYDROBROMIDE
FDA Application No: (ANDA) 077592
Active Ingredient(s): GALANTAMINE HYDROBROMIDE
Company: SUN PHARM INDS
 
Label History
 
Labels are not available on this site for GALANTAMINE HYDROBROMIDE, (ANDA) 077592
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/28/2007 000Tentative Approval  
 
Therapeutic Equivalents
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