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    Sola Pharmaceuticals

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    01 1CARBOPROST TROMETHAMINE

    02 1CYANOCOBALAMIN

    03 2DIMETHYL FUMARATE

    04 2TERIFLUNOMIDE

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    01

    Brand Name : CARBOPROST TROMETHAM...

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

    U.S.A
    AIChE Annual Meeting
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    • fda
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    • WHO-GMP
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    RLD : No

    TE Code : AP

    CARBOPROST TROMETHAMINE

    Sola Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CARBOPROST TROMETHAMINE

    Dosage Strength : EQ 0.25MG BASE/ML

    Approval Date : 2023-05-19

    Application Number : 216824

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : CYANOCOBALAMIN

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

    U.S.A
    AIChE Annual Meeting
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    CYANOCOBALAMIN

    Sola Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CYANOCOBALAMIN

    Dosage Strength : 1MG/ML

    Approval Date : 2022-04-15

    Application Number : 215417

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : DIMETHYL FUMARATE

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

    U.S.A
    AIChE Annual Meeting
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    DIMETHYL FUMARATE

    Sola Pharmaceuticals

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : DIMETHYL FUMARATE

    Dosage Strength : 120MG

    Approval Date : 2021-03-26

    Application Number : 210436

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : DIMETHYL FUMARATE

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

    U.S.A
    AIChE Annual Meeting
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    DIMETHYL FUMARATE

    Sola Pharmaceuticals

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : DIMETHYL FUMARATE

    Dosage Strength : 240MG

    Approval Date : 2021-03-26

    Application Number : 210436

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : TERIFLUNOMIDE

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

    U.S.A
    AIChE Annual Meeting
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    TERIFLUNOMIDE

    Sola Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TERIFLUNOMIDE

    Dosage Strength : 14MG

    Approval Date : 2020-06-17

    Application Number : 209677

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : TERIFLUNOMIDE

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

    U.S.A
    AIChE Annual Meeting
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    • fda
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    RLD : No

    TE Code : AB

    TERIFLUNOMIDE

    Sola Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TERIFLUNOMIDE

    Dosage Strength : 7MG

    Approval Date : 2023-09-28

    Application Number : 209677

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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