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Drugs@FDA: FDA Approved Drug Products
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`Page 1 of 2
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`FDA Approved Drug Products
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`Back} watery;
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`Drug Details
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`Drug Name{5)
`FDA Appiication No.
`Active ingredienfls)
`Company
`Original Approval or Tentative Approval Date
`Chemical Type
`Review Classification
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`FAQ6 i
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`Instructions'7 i Glossary8 l
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`Contact Us9
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`'Email Link
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`RESTASIS
`(NDA) 050793
`CYCLOSPORINE
`ALLERGAN
`December 23, 2002
`3 New dosage form
`i3 Priority review drug
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`a There are no Therapeutic Equivaients
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`- Label Information
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`a Approval History, Letters, Reviews, and
`Related Documents
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`Products on Application (NDA) #050790
`Click on a column header to re-sort the table:
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`Drug Name
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`Active Ingredients
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`Strength
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`Dosage Form/Route
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`RESTASIS
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`CYCLOSPORINE
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`0.05%
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`EMULSION;OPHTHALMIC
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`Marketing
`Status
`Prescription
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`RLD TE
`Code
`Yes None
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`4/14/2015
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`APOTEX
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`1067,pg.1
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`APOTEX 1067, pg. 1
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`

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`Drugs@FDA: FDA Approved Drug Products
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`APOTEX 1067, pg. 2
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