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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    ATNAHS PHARMA UK LIMITED

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    01 1KETOROLAC TROMETHAMINE

    02 6NAPROXEN

    03 2NAPROXEN SODIUM

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    01

    Brand Name : KETOROLAC TROMETHAMI...

    United Kingdom
    AIChE Annual Meeting
    Not Confirmed
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    Brand Name : KETOROLAC TROMETHAMI...

    United Kingdom
    AIChE Annual Meeting
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    RLD : No

    TE Code : AB

    KETOROLAC TROMETHAMINE

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : KETOROLAC TROMETHAMINE

    Dosage Strength : 10MG

    Approval Date : 2022-10-21

    Application Number : 216407

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : NAPROSYN

    United Kingdom
    AIChE Annual Meeting
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    Brand Name : NAPROSYN

    United Kingdom
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    RLD : Yes

    TE Code :

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 250MG

    Approval Date : 1982-01-01

    Application Number : 17581

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    Brand Name : NAPROSYN

    United Kingdom
    AIChE Annual Meeting
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    RLD : Yes

    TE Code :

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 375MG

    Approval Date : 1982-01-01

    Application Number : 17581

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    Brand Name : NAPROSYN

    United Kingdom
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    RLD : Yes

    TE Code : AB

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 500MG

    Approval Date : 1982-04-15

    Application Number : 17581

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    Brand Name : NAPROSYN

    United Kingdom
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    RLD : Yes

    TE Code : AB

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 25MG/ML

    Approval Date : 1987-03-23

    Application Number : 18965

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    Brand Name : EC-NAPROSYN

    United Kingdom
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    Brand Name : EC-NAPROSYN

    United Kingdom
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    RLD : Yes

    TE Code : AB

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : EC-NAPROSYN

    Dosage Strength : 375MG

    Approval Date : 1994-10-14

    Application Number : 20067

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    Brand Name : EC-NAPROSYN

    United Kingdom
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    RLD : Yes

    TE Code : AB

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : EC-NAPROSYN

    Dosage Strength : 500MG

    Approval Date : 1994-10-14

    Application Number : 20067

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    08

    Brand Name : ANAPROX

    United Kingdom
    AIChE Annual Meeting
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    Brand Name : ANAPROX

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    RLD : Yes

    TE Code :

    NAPROXEN SODIUM

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : ANAPROX

    Dosage Strength : EQ 250MG BASE **Federal ...

    Approval Date : 1982-01-01

    Application Number : 18164

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    Brand Name : ANAPROX DS

    United Kingdom
    AIChE Annual Meeting
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    Brand Name : ANAPROX DS

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    RLD : Yes

    TE Code : AB

    NAPROXEN SODIUM

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : ANAPROX DS

    Dosage Strength : EQ 500MG BASE

    Approval Date : 1987-09-30

    Application Number : 18164

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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