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    01 4APIXABAN

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    04 3SITAGLIPTIN PHOSPHATE

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    Brand Name : APIXABAN

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    APIXABAN

    Unichem Laboratories Limited

    Dosage Form : TABLET; FILM COATED

    Proprietary Name : APIXABAN

    Dosage Strength : 1.5MG

    Approval Date :

    Application Number : 210108

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    TE Code :

    APIXABAN

    Unichem Laboratories Limited

    Dosage Form : TABLET; FILM COATED

    Proprietary Name : APIXABAN

    Dosage Strength : 2.0MG

    Approval Date :

    Application Number : 210108

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    TE Code :

    APIXABAN

    Unichem Laboratories Limited

    Dosage Form : TABLET; FILM COATED

    Proprietary Name : APIXABAN

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 210108

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    RLD :

    TE Code :

    APIXABAN

    Unichem Laboratories Limited

    Dosage Form : TABLET; FILM COATED

    Proprietary Name : APIXABAN

    Dosage Strength : 2.5MG

    Approval Date :

    Application Number : 210108

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    05

    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Unichem Laboratories Limited

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 125MG VALPROIC ACID

    Approval Date : 2011-04-05

    Application Number : 79163

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Unichem Laboratories Limited

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 250MG VALPROIC ACID

    Approval Date : 2011-04-05

    Application Number : 79163

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : DIVALPROEX SODIUM

    India
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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Unichem Laboratories Limited

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 500MG VALPROIC ACID

    Approval Date : 2011-04-05

    Application Number : 79163

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : LAMOTRIGINE

    India
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    RLD : No

    TE Code : AB

    LAMOTRIGINE

    Unichem Laboratories Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : LAMOTRIGINE

    Dosage Strength : 25MG

    Approval Date : 2011-10-06

    Application Number : 90170

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : LAMOTRIGINE

    India
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    RLD : No

    TE Code : AB

    LAMOTRIGINE

    Unichem Laboratories Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : LAMOTRIGINE

    Dosage Strength : 100MG

    Approval Date : 2011-10-06

    Application Number : 90170

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : LAMOTRIGINE

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    RLD : No

    TE Code : AB

    LAMOTRIGINE

    Unichem Laboratories Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : LAMOTRIGINE

    Dosage Strength : 150MG

    Approval Date : 2011-10-06

    Application Number : 90170

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Contact Unichem Laboratories Limited and get a quotation

    Unichem Laboratories Limited is a supplier offers 112 products (APIs, Excipients or Intermediates).

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