Label: TRIAMCINOLONE-MOXIFLOXACIN PF suspension

  • 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 February 27, 2018

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  • STORAGE AND HANDLING

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

  • PRINCIPAL DISPLAY PANEL

    Vial Label

  • INGREDIENTS AND APPEARANCE
    TRIAMCINOLONE-MOXIFLOXACIN PF 
    triamcinolone-moxifloxacin pf suspension
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70261-510
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MOXIFLOXACIN HYDROCHLORIDE (UNII: C53598599T) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN1 mg  in 1 mL
    TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE15 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70261-510-010.6 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product01/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2018
    Labeler - ImprimisRx NJ (931390178)