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    Approved Drug Products containing 209777 listed in the FDA Orange Book. Original Data : FDA Website

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    Protega Pharmaceuticals

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    01 PROTEGA PHARMS (3)

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    01 TABLET;ORAL (3)

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    01 RX (3)

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    01 ROXYBOND (3)

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    01 No (3)

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      OXYCODONE HYDROCHLORIDE

      PDF Supplier PDF
      URL Supplier Web Content
      TABLET; ORAL
      15MG
      2017-04-20
      209777
      ROXYBOND
      RX
      No
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        OXYCODONE HYDROCHLORIDE

        PDF Supplier PDF
        URL Supplier Web Content
        TABLET; ORAL
        30MG
        2017-04-20
        209777
        ROXYBOND
        RX
        No
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          OXYCODONE HYDROCHLORIDE

          PDF Supplier PDF
          URL Supplier Web Content
          TABLET; ORAL
          5MG
          2017-04-20
          209777
          ROXYBOND
          RX
          No
          ASK
          US
          PHARMACOMPASS
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          your Marketing & Sales content

          Looking for FDA Orange Book APPLICATION 209777

          Looking for FDA Orange Book APPLICATION 209777 3

          19

          Protega Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

          One of their notable products is OXYCODONE HYDROCHLORIDE, with a corresponding application number 209777.

          Regulatory Information RX

          With a dosage strength 15MG

          Dosage Form Route TABLET; ORAL

          Reference Listed Drug No

          Approved since 2017-04-20

          18

          Protega Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

          One of their notable products is OXYCODONE HYDROCHLORIDE, with a corresponding application number 209777.

          Regulatory Information RX

          With a dosage strength 30MG

          Dosage Form Route TABLET; ORAL

          Reference Listed Drug No

          Approved since 2017-04-20

          17

          Protega Pharmaceuticals, based in U.S.A, is a pharmaceutical company.

          One of their notable products is OXYCODONE HYDROCHLORIDE, with a corresponding application number 209777.

          Regulatory Information RX

          With a dosage strength 5MG

          Dosage Form Route TABLET; ORAL

          Reference Listed Drug No

          Approved since 2017-04-20

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