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    Drug Product Composition: Pasireotide Diaspartate

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    Pasireotide Diaspartate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

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    USFDA APPLICATION NUMBER - 200677 / DOSAGE - SOLUTION;SUBCUTANEOUS - EQ 0.6MG BASE/ML (EQ 0.6MG BASE/ML)

    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PASIREOTIDE(UNII: 98H1T17066)
    (PASIREOTIDE - UNII:98H1T17066)     		PASIREOTIDE0.9mg in 1 | 0.6mg in 1 | 0.3mg in 1

    Inactive Ingredients

    Ingredient Name
    Novartis Pharmaceuticals Corporation
    MANNITOL(3OWL53L36A)
    SODIUM HYDROXIDE(55X04QC32I)
    TARTARIC ACID(W4888I119H)
    WATER(059QF0KO0R)