Label: MOXIFLOXACIN PF injection, solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated March 3, 2020

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  • STORAGE AND HANDLING

    Store at 20° to 25° C (68° to 77° F)

  • Package Label

    Package Label

  • INGREDIENTS AND APPEARANCE
    MOXIFLOXACIN PF 
    moxifloxacin pf injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:71384-509
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN5 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71384-509-0120 in 1 BOX02/10/2020
    11 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/10/2020
    Labeler - Imprimis NJOF, LLC (080431967)
    Registrant - Imprimis NJOF, LLC (080431967)