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    Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

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    01 5AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    02 2DEXMETHYLPHENIDATE HYDROCHLORIDE

    03 12LEVOTHYROXINE SODIUM

    04 3METHYLPHENIDATE HYDROCHLORIDE

    05 3OSELTAMIVIR PHOSPHATE

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    01

    Brand Name : DEXTROAMP SACCHARATE...

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    AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXTROAMP SACCHARATE, AMP...

    Dosage Strength : 1.25MG;1.25MG;1.25MG;1...

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    Approval Date : 2022-07-05

    Application Number : 210754

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : DEXTROAMP SACCHARATE...

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    AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXTROAMP SACCHARATE, AMP...

    Dosage Strength : 2.5MG;2.5MG;2.5MG;2.5M...

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    Approval Date : 2022-07-05

    Application Number : 210754

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : DEXTROAMP SACCHARATE...

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    AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXTROAMP SACCHARATE, AMP...

    Dosage Strength : 3.75MG;3.75MG;3.75MG;3...

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    Approval Date : 2022-07-05

    Application Number : 210754

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    04

    Brand Name : DEXTROAMP SACCHARATE...

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    AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXTROAMP SACCHARATE, AMP...

    Dosage Strength : 5MG;5MG;5MG;5MG

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    Approval Date : 2022-07-05

    Application Number : 210754

    Regulatory Info : RX

    Registration Country : USA

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    05

    Brand Name : DEXTROAMP SACCHARATE...

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    AIChE Annual Meeting
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    AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXTROAMP SACCHARATE, AMP...

    Dosage Strength : 7.5MG;7.5MG;7.5MG;7.5M...

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    Approval Date : 2022-07-05

    Application Number : 210754

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : DEXMETHYLPHENIDATE H...

    U.S.A
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    Brand Name : DEXMETHYLPHENIDATE H...

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    Regulatory Info : RX

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXMETHYLPHENIDATE HYDROC...

    Dosage Strength : 5MG

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    Approval Date : 2018-09-19

    Application Number : 209211

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : DEXMETHYLPHENIDATE H...

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    Regulatory Info : RX

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : DEXMETHYLPHENIDATE HYDROC...

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2018-09-19

    Application Number : 209211

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : LEVO-T

    U.S.A
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    Regulatory Info : RX

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    LEVOTHYROXINE SODIUM

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : LEVO-T

    Dosage Strength : 0.025MG **See current ...

    Packaging :

    Approval Date : 2002-03-01

    Application Number : 21342

    Regulatory Info : RX

    Registration Country : USA

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    09

    Brand Name : LEVO-T

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    Regulatory Info : RX

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    LEVOTHYROXINE SODIUM

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : LEVO-T

    Dosage Strength : 0.05MG **See current A...

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    Approval Date : 2002-03-01

    Application Number : 21342

    Regulatory Info : RX

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    10

    Brand Name : LEVO-T

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    Regulatory Info : RX

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    LEVOTHYROXINE SODIUM

    Neolpharma

    Dosage Form : TABLET;ORAL

    Brand Name : LEVO-T

    Dosage Strength : 0.075MG **See current ...

    Packaging :

    Approval Date : 2002-03-01

    Application Number : 21342

    Regulatory Info : RX

    Registration Country : USA

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