Visitor Monitoring Drug Details: OPTIRAY 350
 
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Drug Details

Drug Name: OPTIRAY 350
FDA Application No: (NDA) 020923
Active Ingredient(s): IOVERSOL
Company: MALLINCKRODT
Original Approval or Tentative Approval Date: May 29, 1998
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
OPTIRAY 240 IOVERSOL51%INJECTABLE; INJECTION Discontinued No None
OPTIRAY 300 IOVERSOL64%INJECTABLE; INJECTION Prescription Yes None
OPTIRAY 320 IOVERSOL68%INJECTABLE; INJECTION Discontinued No None
OPTIRAY 350 IOVERSOL74%INJECTABLE; INJECTION Prescription Yes None


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