Label: DELTASONE- prednisone tablet

  • NDC Code(s): 69668-120-20
  • Packager: Oculus Innovative Sciences
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 7, 2017

If you are a consumer or patient please visit this version.

  • Warnings

    Warnings: Keep this product out of reach
    of children. In case of accidental overdose,
    call a doctor or poison control center
    immediately.
    All prescriptions using this product shall be
    pursuant to state statutes as applicable.
    This product may be administered only
    under a physician’s supervision.
    Call your doctor about side effects.
    You may report side effects to FDA at
    1-800-FDA-1088.

  • Deltasone 20mg

    Detasone 20mg

  • INGREDIENTS AND APPEARANCE
    DELTASONE 
    prednisone tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69668-120
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) PREDNISONE20 mg  in 20 mg
    Product Characteristics
    ColororangeScore2 pieces
    ShapeROUNDSize9mm
    FlavorImprint Code Westward;477
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69668-120-2020 mg in 1 BOTTLE; Type 0: Not a Combination Product08/31/2015
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA08367708/03/2009
    Labeler - Oculus Innovative Sciences (081642964)