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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Contract Pharmacal Corporation

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    01 2CETIRIZINE HYDROCHLORIDE

    02 2CIMETIDINE

    03 4FAMOTIDINE

    04 2FEXOFENADINE HYDROCHLORIDE

    05 1FOLIC ACID

    06 9IBUPROFEN

    07 1IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

    08 1LOPERAMIDE HYDROCHLORIDE

    09 2NAPROXEN SODIUM

    10 1PREDNISONE

    11 1QUINIDINE SULFATE

    12 1RANITIDINE HYDROCHLORIDE

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    01

    Brand Name : CETIRIZINE HYDROCHLO...

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    Brand Name : CETIRIZINE HYDROCHLO...

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    RLD : No

    TE Code :

    CETIRIZINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : CETIRIZINE HYDROCHLORIDE...

    Dosage Strength : 5MG

    Approval Date : 2007-12-27

    Application Number : 76047

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    02

    Brand Name : CETIRIZINE HYDROCHLO...

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    RLD : No

    TE Code :

    CETIRIZINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : CETIRIZINE HYDROCHLORIDE...

    Dosage Strength : 10MG

    Approval Date : 2007-12-27

    Application Number : 76047

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    Brand Name : CIMETIDINE

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    RLD : No

    TE Code :

    CIMETIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : CIMETIDINE

    Dosage Strength : 200MG

    Approval Date : 1998-06-19

    Application Number : 74961

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : CIMETIDINE

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    RLD : No

    TE Code :

    CIMETIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : CIMETIDINE

    Dosage Strength : 200MG

    Approval Date : 1998-06-19

    Application Number : 74963

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : FAMOTIDINE

    U.S.A
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    RLD : No

    TE Code : AB

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 20MG

    Approval Date : 2023-12-20

    Application Number : 217669

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : FAMOTIDINE

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    RLD : No

    TE Code : AB

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 40MG

    Approval Date : 2023-12-20

    Application Number : 217669

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : FAMOTIDINE

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    RLD : No

    TE Code :

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 10MG

    Approval Date : 2024-05-28

    Application Number : 218003

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    08

    Brand Name : FAMOTIDINE

    U.S.A
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    RLD : No

    TE Code :

    FAMOTIDINE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 20MG

    Approval Date : 2024-05-28

    Application Number : 218003

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    09

    Brand Name : FEXOFENADINE HYDROCH...

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Brand Name : FEXOFENADINE HYDROCH...

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    RLD : No

    TE Code :

    FEXOFENADINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FEXOFENADINE HYDROCHLORI...

    Dosage Strength : 60MG

    Approval Date : 2025-02-28

    Application Number : 219032

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    10

    Brand Name : FEXOFENADINE HYDROCH...

    U.S.A
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    RLD : No

    TE Code :

    FEXOFENADINE HYDROCHLORIDE

    Contract Pharmacal Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : FEXOFENADINE HYDROCHLORI...

    Dosage Strength : 180MG

    Approval Date : 2025-02-28

    Application Number : 219032

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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