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`Drug Details
`
`Drug Name(s)
`FDA Application No.
`Active Ingredient(s)
`Company
`Original Approval or Tentative Approval Date
`Chemical Type
`Review Classification
`
`PROFENAL
`(NDA) 019387
`SUPROFEN
`ALCON
`December 23, 1988
`3 New dosage form
`S Standard review drug
`
`(cid:122) There are no Therapeutic Equivalents
`
`(cid:122) Labels are not available
`
`(cid:122) Approval History, Letters, Reviews, and
`Related Documents
`
`Products on Application (NDA) #019387
` Click on a column header to re-sort the table:
`
`Drug Name
`
`Active Ingredients
`
`Strength Dosage Form/Route
`
`PROFENAL
`
`SUPROFEN
`
`1%
`
`SOLUTION/DROPS;OPHTHALMIC
`
`Marketing
`Status
`Discontinued
`
`RLD TE
`Code
`No None
`
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