Visitor Monitoring Drug History: PALLADONE
 
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Label and Approval History

Drug Name: PALLADONE
FDA Application No: (NDA) 021044
Active Ingredient(s): HYDROMORPHONE HYDROCHLORIDE
Company: PURDUE PHARMA LP
 
Label History
 
View the label approved on September 24, 2004 for PALLADONE, (NDA) 021044


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/24/2004 000Approval Letter
Label
Review
Other Important Information from FDA 
 
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