Label: ORBIFLOXACIN powder

  • NDC Code(s): 38217-2328-1
  • Packager: Sumitomo Dainippon Pharma Co., Ltd.
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: bulk ingredient

Drug Label Information

Updated November 16, 2018

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  • CAUTION

    For manufacturing

    For manufacturing, processing, or repacking

    Federal law restricts this drug to use by or on the order of a licensed veterinarian. Store at 4°C to 30°C, with excursions up to 50°C.

    LOT NO.: GROSS: kg

                      TARE: kg

    RETEST DATE: NET: kg

    Sumitomo Dainippon Pharma Co., Ltd.

    1450 Yasuzuka – Cho, Suzuka, Mie, 513-0818, Japan

    Orbifloxacin Bulk Ingredient
  • INGREDIENTS AND APPEARANCE
    ORBIFLOXACIN 
    orbifloxacin powder
    Product Information
    Product TypeItem Code (Source)NDC:38217-2328
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    orbifloxacin (UNII: 660932TPY6) (orbifloxacin - UNII:660932TPY6) orbifloxacin1 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:38217-2328-130 kg in 1 DRUM
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient08/05/1997
    Labeler - Sumitomo Dainippon Pharma Co., Ltd. (690555636)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sumitomo Dainippon Pharma Co., Ltd.706295235API MANUFACTURE, PACK, LABEL, ANALYSIS