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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Sulfadiazine

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1ABBVIE

    02 1CHARTWELL MOLECULAR

    03 1EPIC PHARMA LLC

    04 1EVERYLIFE

    05 1IMPAX LABS

    06 2LEDERLE

    07 2LILLY

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    01

    ABBVIE

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    RLD : No

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 300MG

    Approval Date : 1982-01-01

    Application Number : 4125

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Abbvie Company Banner

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    02

    CHARTWELL MOLECULAR

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    CHARTWELL MOLECULAR

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    RLD : No

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 80084

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    LILLY

    U.S.A
    euroPLX 86 Munich
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    LILLY

    U.S.A
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    euroPLX 86 Munich
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    RLD : Yes

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 4122

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    LILLY

    U.S.A
    euroPLX 86 Munich
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    LILLY

    U.S.A
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    euroPLX 86 Munich
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    RLD : No

    TE Code :

    SULFADIAZINE; SULFAMERAZINE

    Brand Name : SULFONAMIDES DUPLEX

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 250MG/5ML;250MG/5ML

    Approval Date : 1982-01-01

    Application Number : 6317

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    05

    EPIC PHARMA LLC

    U.S.A
    euroPLX 86 Munich
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    EPIC PHARMA LLC

    U.S.A
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    euroPLX 86 Munich
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    RLD : No

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1994-07-29

    Application Number : 40091

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

    blank

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    06

    EVERYLIFE

    United Kingdom
    euroPLX 86 Munich
    Not Confirmed
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    EVERYLIFE

    United Kingdom
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    euroPLX 86 Munich
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    RLD : No

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 80088

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    IMPAX LABS

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    IMPAX LABS

    U.S.A
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    euroPLX 86 Munich
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    RLD : Yes

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 80081

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    08

    LEDERLE

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    LEDERLE

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    SULFADIAZINE

    Brand Name : SULFADIAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 4054

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    LEDERLE

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
    arrow

    LEDERLE

    U.S.A
    arrow
    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    SULFADIAZINE SODIUM

    Brand Name : SULFADIAZINE SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

    Approval Date : 1982-01-01

    Application Number : 4054

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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