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    Nexgen Pharma, Inc.

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    01 1BROMPHENIRAMINE MALEATE

    02 1DIMENHYDRINATE

    03 1DIPHENHYDRAMINE HYDROCHLORIDE

    04 1FOLIC ACID

    05 1HYDROCORTISONE

    06 1ISONIAZID

    07 1MECLIZINE HYDROCHLORIDE

    08 2MEPROBAMATE

    09 1PENTOBARBITAL SODIUM

    10 1PHENDIMETRAZINE TARTRATE

    11 1POLYETHYLENE GLYCOL 3350

    12 1PROPOXYPHENE HYDROCHLORIDE

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    01

    Brand Name : BROMPHENIRAMINE MALE...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : BROMPHENIRAMINE MALE...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    BROMPHENIRAMINE MALEATE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : BROMPHENIRAMINE MALEATE

    Dosage Strength : 4MG

    Approval Date : 1982-01-01

    Application Number : 86187

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : DIMENHYDRINATE

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : DIMENHYDRINATE

    U.S.A
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    RLD : No

    TE Code :

    DIMENHYDRINATE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : DIMENHYDRINATE

    Dosage Strength : 50MG

    Approval Date : 1982-01-01

    Application Number : 85985

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : DIPHENHYDRAMINE HYDR...

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

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    RLD : No

    TE Code :

    DIPHENHYDRAMINE HYDROCHLORIDE

    Nexgen Pharma, Inc.

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : DIPHENHYDRAMINE HYDROCHL...

    Dosage Strength : 25MG

    Approval Date : 1982-01-01

    Application Number : 83634

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : FOLIC ACID

    U.S.A
    Fi Europe 2024
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    Brand Name : FOLIC ACID

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    RLD : No

    TE Code :

    FOLIC ACID

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : FOLIC ACID

    Dosage Strength : 1MG

    Approval Date : 1982-01-01

    Application Number : 84915

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : HYDROCORTISONE

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : HYDROCORTISONE

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    RLD : No

    TE Code :

    HYDROCORTISONE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : HYDROCORTISONE

    Dosage Strength : 20MG

    Approval Date : 1982-01-01

    Application Number : 83140

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    06

    Brand Name : ISONIAZID

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : ISONIAZID

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    RLD : No

    TE Code :

    ISONIAZID

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : ISONIAZID

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 84050

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : MECLIZINE HYDROCHLOR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : MECLIZINE HYDROCHLOR...

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    RLD : No

    TE Code :

    MECLIZINE HYDROCHLORIDE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET, CHEWABLE; ORAL

    Proprietary Name : MECLIZINE HYDROCHLORIDE

    Dosage Strength : 25MG

    Approval Date : 1982-01-01

    Application Number : 86392

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    Brand Name : MEPROBAMATE

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : MEPROBAMATE

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    RLD : No

    TE Code :

    MEPROBAMATE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : MEPROBAMATE

    Dosage Strength : 200MG

    Approval Date : 1982-01-01

    Application Number : 84220

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    Brand Name : MEPROBAMATE

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : MEPROBAMATE

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    RLD : No

    TE Code :

    MEPROBAMATE

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : MEPROBAMATE

    Dosage Strength : 400MG

    Approval Date : 1982-01-01

    Application Number : 84589

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    Brand Name : SODIUM PENTOBARBITAL

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : SODIUM PENTOBARBITAL

    U.S.A
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Nexgen Pharma, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : SODIUM PENTOBARBITAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 84238

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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