Label: DOXYCYCLINE tablet, film coated

  • NDC Code(s): 51376-780-10
  • Packager: Blessings International
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated January 22, 2020

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  • PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label

    BLESSINGS
    INTERNATIONAL®
    MEDICINESFORMISSIONS

    NDC 51376-780-10

    Doxycycline

    100 mg

    1,000 Film Coated Tablets USP

    RX ONLY / FOR EXPORT ONLY

    PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label
  • INGREDIENTS AND APPEARANCE
    DOXYCYCLINE 
    doxycycline tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:51376-780
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Doxycycline (UNII: N12000U13O) (DOXYCYCLINE ANHYDROUS - UNII:334895S862) DOXYCYCLINE ANHYDROUS100 mg
    Inactive Ingredients
    Ingredient NameStrength
    Magnesium Stearate (UNII: 70097M6I30)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Methylene Chloride (UNII: 588X2YUY0A)  
    Microcrystalline Cellulose (UNII: OP1R32D61U)  
    Talc (UNII: 7SEV7J4R1U)  
    Starch, Potato (UNII: 8I089SAH3T)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code DOXYC
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51376-780-101000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only05/01/2008
    Labeler - Blessings International (064965742)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blessings International064965742MANUFACTURE(51376-780)