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    Adalat XL

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    BAYER PHARMS

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    Virtual BoothBayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.

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    RLD : No

    TE Code :

    NIFEDIPINE

    Brand Name : ADALAT

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 10MG

    Approval Date : 1985-11-27

    Application Number : 19478

    RX/OTC/DISCN : DISCN

    RLD : No

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    BAYER PHARMS

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    RLD : No

    TE Code :

    NIFEDIPINE

    Brand Name : ADALAT

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 20MG

    Approval Date : 1986-09-17

    Application Number : 19478

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    NORWICH

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    Brand Name : ADALAT CC

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1993-04-21

    Application Number : 20198

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    NORWICH

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    Brand Name : ADALAT CC

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1993-04-21

    Application Number : 20198

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    NORWICH

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    Brand Name : ADALAT CC

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1993-04-21

    Application Number : 20198

    RX/OTC/DISCN : DISCN

    RLD : Yes

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    06

    PFIZER

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    Brand Name : PROCARDIA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 10MG

    Approval Date : 1982-01-01

    Application Number : 18482

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    PFIZER

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    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**

    Approval Date : 1986-07-24

    Application Number : 18482

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    PFIZER

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    RLD : Yes

    TE Code : AB2

    NIFEDIPINE

    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

    Approval Date : 1989-09-06

    Application Number : 19684

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB2

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    09

    PFIZER

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    RLD : Yes

    TE Code : AB2

    NIFEDIPINE

    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 60MG

    Approval Date : 1989-09-06

    Application Number : 19684

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB2

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    10

    PFIZER

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    RLD : Yes

    TE Code :

    NIFEDIPINE

    Brand Name : PROCARDIA XL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 90MG

    Approval Date : 1989-09-06

    Application Number : 19684

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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