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`Drug Details
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`Drug Name(s)
`FDA Application No.
`Active Ingredient(s)
`Company
`Original Approval or Tentative Approval Date
`Chemical Type
`Review Classification
`
`VOLTAREN
`(NDA) 020037
`DICLOFENAC SODIUM
`NOVARTIS
`March 28, 1991
`3 New dosage form
`P Priority review drug
`
`(cid:122) Therapeutic Equivalents
`
`(cid:122) Label Information
`
`(cid:122) Approval History, Letters, Reviews, and
`Related Documents
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`Products on Application (NDA) #020037
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`Drug Name
`
`Active Ingredients
`
`Strength Dosage Form/Route
`
`VOLTAREN
`
`DICLOFENAC SODIUM
`
`0.1%
`
`SOLUTION/DROPS;OPHTHALMIC
`
`Marketing
`Status
`Prescription
`
`RLD TE
`Code
`Yes AT
`
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