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    Omnivium Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1CLEMASTINE FUMARATE

    02 1COCAINE HYDROCHLORIDE

    03 1GLYCOPYRROLATE

    04 2ISONIAZID

    05 2ISOSORBIDE MONONITRATE

    06 1SODIUM BICARBONATE

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    01

    Brand Name : CLEMASTINE FUMARATE

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    AIChE Annual Meeting
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    Brand Name : CLEMASTINE FUMARATE

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    RLD : No

    TE Code :

    CLEMASTINE FUMARATE

    Omnivium Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : CLEMASTINE FUMARATE

    Dosage Strength : 2.68MG

    Approval Date : 1993-10-31

    Application Number : 73459

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : NUMBRINO

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    Brand Name : NUMBRINO

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    RLD : Yes

    TE Code :

    COCAINE HYDROCHLORIDE

    Omnivium Pharmaceuticals

    Dosage Form : SOLUTION; NASAL

    Proprietary Name : NUMBRINO

    Dosage Strength : 4%

    Approval Date : 2020-01-10

    Application Number : 209575

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : GLYCOPYRROLATE

    U.S.A
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    Brand Name : GLYCOPYRROLATE

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    RLD : No

    TE Code : AP

    GLYCOPYRROLATE

    Omnivium Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : GLYCOPYRROLATE

    Dosage Strength : 0.2MG/ML

    Approval Date : 2022-11-29

    Application Number : 212871

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    Brand Name : ISONIAZID

    U.S.A
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    RLD : No

    TE Code : AA

    ISONIAZID

    Omnivium Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ISONIAZID

    Dosage Strength : 100MG

    Approval Date : 1997-06-26

    Application Number : 40090

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    05

    Brand Name : ISONIAZID

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    RLD : No

    TE Code : AA

    ISONIAZID

    Omnivium Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ISONIAZID

    Dosage Strength : 300MG

    Approval Date : 1997-06-26

    Application Number : 40090

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    06

    Brand Name : MONOKET

    U.S.A
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    Brand Name : MONOKET

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    RLD : Yes

    TE Code : AB

    ISOSORBIDE MONONITRATE

    Omnivium Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : MONOKET

    Dosage Strength : 20MG

    Approval Date : 1993-06-30

    Application Number : 20215

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    Brand Name : MONOKET

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    Brand Name : MONOKET

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    RLD : Yes

    TE Code : AB

    ISOSORBIDE MONONITRATE

    Omnivium Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : MONOKET

    Dosage Strength : 10MG

    Approval Date : 1993-06-30

    Application Number : 20215

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    08

    Brand Name : SODIUM BICARBONATE

    U.S.A
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    Brand Name : SODIUM BICARBONATE

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    RLD : No

    TE Code : AP

    SODIUM BICARBONATE

    Omnivium Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SODIUM BICARBONATE

    Dosage Strength : 1MEQ/ML

    Approval Date : 2023-06-15

    Application Number : 216364

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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