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    Trusted Global CDMO Partner Delivering End-to-End Pharma Manufacturing & Development Solutions.

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    Evonik Health Care is the innovation hub for leading life science companies

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    Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.

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    Axplora is your partner of choice for complex APIs.

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

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    Pfizer Inc

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    Brand Name : SOLU-CORTEF

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    RLD : Yes

    TE Code :

    HYDROCORTISONE SODIUM SUCCINATE

    Pfizer Inc

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SOLU-CORTEF

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 1982-01-01

    Application Number : 9866

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    Brand Name : SOLU-CORTEF

    U.S.A
    BePharma
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    Brand Name : SOLU-CORTEF

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    RLD : Yes

    TE Code : AP

    HYDROCORTISONE SODIUM SUCCINATE

    Pfizer Inc

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SOLU-CORTEF

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 1982-01-01

    Application Number : 9866

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    Brand Name : SOLU-CORTEF

    U.S.A
    BePharma
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    Brand Name : SOLU-CORTEF

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    RLD : Yes

    TE Code :

    HYDROCORTISONE SODIUM SUCCINATE

    Pfizer Inc

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SOLU-CORTEF

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 1982-01-01

    Application Number : 9866

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : SOLU-CORTEF

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    BePharma
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    Brand Name : SOLU-CORTEF

    U.S.A
    BePharma
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    HYDROCORTISONE SODIUM SUCCINATE

    Pfizer Inc

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : SOLU-CORTEF

    Dosage Strength : EQ 250MG BASE/VIAL

    Approval Date : 1982-01-01

    Application Number : 9866

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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