Visitor Monitoring Drug Details: ORAMORPH SR
 
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Drug Details

Drug Name: ORAMORPH SR
FDA Application No: (NDA) 019977
Active Ingredient(s): MORPHINE SULFATE
Company: XANODYNE PHARM
Original Approval or Tentative Approval Date: August 15, 1991
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ORAMORPH SR MORPHINE SULFATE30MGTABLET, EXTENDED RELEASE; ORAL Prescription No BC
ORAMORPH SR MORPHINE SULFATE60MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes BC
ORAMORPH SR MORPHINE SULFATE100MGTABLET, EXTENDED RELEASE; ORAL Prescription No BC
ORAMORPH SR MORPHINE SULFATE15MGTABLET, EXTENDED RELEASE; ORAL Prescription No BC


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