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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    End-to-end drug development, specializing in high-potency softgels and liquids, providing global partners with a competitive advantage.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    Nifedipine

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    Brand Name : Adco-Vascard 30 SR

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    Brand Name : ADALAT CC

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    Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1993-04-21

    Application Number : 20198

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    NIFEDIPINE

    Brand Name : ADALAT CC

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    Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1993-04-21

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    Brand Name : ADALAT

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    Approval Date : 1985-11-27

    Application Number : 19478

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    NIFEDIPINE

    Brand Name : ADALAT

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 1986-09-17

    Application Number : 19478

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    Nifedipine

    Brand Name : Adalat Retard 20

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    Brand Name : Gitsalat 60

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    Brand Name : Adalat XL 30

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    Brand Name : Adalat XL 30

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    Brand Name : Adalat XL 60

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    NIFEDIPINE

    Brand Name : PROCARDIA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1982-01-01

    Application Number : 18482

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    Brand Name : PROCARDIA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1986-07-24

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    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 1989-09-06

    Application Number : 19684

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    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 60MG

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    Approval Date : 1989-09-06

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    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 90MG

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    Approval Date : 1989-09-06

    Application Number : 19684

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