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    FDA Drug Approval, A077419, POTASSIUM CHLORIDE

    FDA Drug Approval, A077419, POTASSIUM CHLORIDE

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    Contents: Summary Basis of Approval

    ANDA: 077419
    Company: ACTAVIS LABS FL INC
    Drug Name: POTASSIUM CHLORIDE
    Active Ingredients: POTASSIUM CHLORIDE
    Strength: 10MEQ
    Dosage Form/Route: CAPSULE, EXTENDED RELEASE;ORAL
    Action Date: 06/02/2008
    Marketing Status: Prescription
    Submission Classification: ORIG-1 TE Code: AB

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