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`EXHIBIT 1012EXHIBIT 1012
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`Drugs@FDA: FDA Approved Drug Products
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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
`
`LOESTRIN FE 1/20
`(NDA) 017354
`ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
`WARNER CHILCOTT
`April 30, 1973
`3 New dosage form
`P Priority review drug
`
`(cid:122) Therapeutic Equivalents
`
`(cid:122) Labels are not available
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`(cid:122) Approval History, Letters, Reviews, and
`Related Documents
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`Products on Application (NDA) #017354
` Click on a column header to re-sort the table:
`
`Drug Name
`
`Active Ingredients
`
`LOESTRIN FE
`1/20
`
`ETHINYL ESTRADIOL; NORETHINDRONE
`ACETATE
`
`Strength
`
`0.02MG;
`1MG
`
`Dosage
`Form/Route
`TABLET;ORAL-28
`
`RLDTE
`Marketing
`Code
`Status
`Prescription No AB
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`Petitioner Exhibit 1012
`Petition for Inter Partes Review of U.S. Patent No. 7,704,984
`Page 1
`2/2/2015
`http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.DrugD...
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`Drugs@FDA: FDA Approved Drug Products
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`Page 2 of 2
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`Petitioner Exhibit 1012
`Petition for Inter Partes Review of U.S. Patent No. 7,704,984
`Page 2
`2/2/2015
`http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.DrugD...