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    p-Isobutylhydratropic acid

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    ABBVIE

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    RLD : Yes

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    HYDROCODONE BITARTRATE; IBUPROFEN

    Brand Name : VICOPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1997-09-23

    Application Number : 20716

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    RLD : No

    TE Code :

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG

    Approval Date : 2001-12-12

    Application Number : 75661

    RX/OTC/DISCN : OTC

    RLD : No

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    RLD : No

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    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 400MG

    Approval Date : 1985-08-06

    Application Number : 70329

    RX/OTC/DISCN : DISCN

    RLD : No

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

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    RLD : No

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    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG

    Approval Date : 2010-12-10

    Application Number : 79174

    RX/OTC/DISCN : OTC

    RLD : No

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    Granules India

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 400MG

    Approval Date : 2001-11-14

    Application Number : 75682

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    DR REDDYS LA

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 600MG

    Approval Date : 2001-11-14

    Application Number : 75682

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    DR REDDYS LA

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 800MG

    Approval Date : 2001-11-14

    Application Number : 75682

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    DR REDDYS LABS INC

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 400MG

    Approval Date : 2001-10-31

    Application Number : 76112

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    DR REDDYS LABS INC

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 600MG

    Approval Date : 2001-10-31

    Application Number : 76112

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    DR REDDYS LABS INC

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    RLD : No

    TE Code : AB

    IBUPROFEN

    Brand Name : IBUPROFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 800MG

    Approval Date : 2001-10-31

    Application Number : 76112

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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