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

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    01 2DIPHENHYDRAMINE HYDROCHLORIDE

    02 1DOXYLAMINE SUCCINATE

    03 3IBUPROFEN

    04 1LOPERAMIDE HYDROCHLORIDE

    05 1METRONIDAZOLE

    06 1NAPROXEN SODIUM

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    01

    Brand Name : DIPHENHYDRAMINE HYDR...

    U.S.A
    AIChE Annual Meeting
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    Brand Name : DIPHENHYDRAMINE HYDR...

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    RLD : No

    TE Code :

    DIPHENHYDRAMINE HYDROCHLORIDE

    LNK

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : DIPHENHYDRAMINE HYDROCHL...

    Dosage Strength : 25MG

    Approval Date : 1983-01-27

    Application Number : 87977

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    02

    Brand Name : DIPHENHYDRAMINE HYDR...

    U.S.A
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    Brand Name : DIPHENHYDRAMINE HYDR...

    U.S.A
    AIChE Annual Meeting
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    RLD : No

    TE Code :

    DIPHENHYDRAMINE HYDROCHLORIDE

    LNK

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : DIPHENHYDRAMINE HYDROCHL...

    Dosage Strength : 50MG

    Approval Date : 1983-01-27

    Application Number : 87978

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : DOXYLAMINE SUCCINATE

    U.S.A
    AIChE Annual Meeting
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    Brand Name : DOXYLAMINE SUCCINATE

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    RLD : No

    TE Code :

    DOXYLAMINE SUCCINATE

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    Dosage Form : TABLET; ORAL

    Proprietary Name : DOXYLAMINE SUCCINATE

    Dosage Strength : 25MG

    Approval Date : 2004-08-27

    Application Number : 40564

    RX/OTC/DISCN : OTC

    RLD : No

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    04

    Brand Name : IBUPROFEN

    U.S.A
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    RLD : No

    TE Code :

    IBUPROFEN

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : IBUPROFEN

    Dosage Strength : 200MG

    Approval Date : 1999-03-01

    Application Number : 75010

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    05

    Brand Name : IBUPROFEN

    U.S.A
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    RLD : No

    TE Code :

    IBUPROFEN

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : IBUPROFEN

    Dosage Strength : 200MG

    Approval Date : 1999-03-01

    Application Number : 75139

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    06

    Brand Name : IBUPROFEN

    U.S.A
    AIChE Annual Meeting
    Not Confirmed
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    Brand Name : IBUPROFEN

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    RLD : No

    TE Code :

    IBUPROFEN

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : IBUPROFEN

    Dosage Strength : 100MG

    Approval Date : 2004-06-17

    Application Number : 76741

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : LOPERAMIDE HYDROCHLO...

    U.S.A
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    Brand Name : LOPERAMIDE HYDROCHLO...

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    RLD : No

    TE Code :

    LOPERAMIDE HYDROCHLORIDE

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : LOPERAMIDE HYDROCHLORIDE

    Dosage Strength : 2MG

    Approval Date : 2003-06-10

    Application Number : 76497

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

    blank

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    08

    Brand Name : METRONIDAZOLE

    U.S.A
    AIChE Annual Meeting
    Not Confirmed
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    Brand Name : METRONIDAZOLE

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    RLD : No

    TE Code :

    METRONIDAZOLE

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : METRONIDAZOLE

    Dosage Strength : 250MG

    Approval Date : 1984-04-10

    Application Number : 19029

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    Brand Name : NAPROXEN SODIUM

    U.S.A
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    Brand Name : NAPROXEN SODIUM

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    RLD : No

    TE Code :

    NAPROXEN SODIUM

    LNK

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROXEN SODIUM

    Dosage Strength : 220MG

    Approval Date : 2017-01-23

    Application Number : 204872

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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