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    FDA Drug Approval, A061667, VANCOCIN HYDROCHLORIDE

    FDA Drug Approval, A061667, VANCOCIN HYDROCHLORIDE

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    Contents: Summary Basis of Approval for all the prior approval supplements during this period (year the request was made: 2019)

    ANDA: 061667
    Company: ANI PHARMS
    Drug Name: VANCOCIN HYDROCHLORIDE
    Active Ingredients: VANCOMYCIN HYDROCHLORIDE
    Strength: EQ 250MG BASE/5ML
    Dosage Form/Route: FOR SOLUTION;ORAL
    Action Date: 07/13/1983
    Marketing Status: Prescription
    Submission Classification: ORIG-1 TE Code: AA
    • Status: Pending Fast-Track Request
    • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

    NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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