Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 68788-7602-1, 68788-7602-2, 68788-7602-3, 68788-7602-4, view more
    68788-7602-5, 68788-7602-6, 68788-7602-7, 68788-7602-8, 68788-7602-9
  • Packager: Preferred Pharmaceuticals Inc.
  • This is a repackaged label.
  • Source NDC Code(s): 49483-603
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated February 14, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ibuprofen tablets 400 mg - 600 mg- 800 mg medguide

    MEDGUIDE IBUPROFEN TABLETS
    Repackaged By: Preferred Pharmaceuticals Inc.

  • HOW SUPPLIED

    600mg (white to off white, capsule shaped, biconvex, film coated tablets debossed with '122' on one side and plain on the other side)

     
    Bottles of 14 NDC 68788-7602-4
     
    Bottles of 20 NDC 68788-7602-2
     
    Bottles of 21 NDC 68788-7602-7
     
    Bottles of 30 NDC 68788-7602-3
     
    Bottles of 50 NDC 68788-7602-5
     
    Bottles of 60 NDC 68788-7602-6
     
    Bottles of 90 NDC 68788-7602-9
     
    Bottles of100 NDC 68788-7602-1
     
    Bottles of 120 NDC 68788-7602-8

    Repackaged By: Preferred Pharmaceuticals Inc.

  • 600mg Label

    Ibuprofen Tablets 600mg
  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:68788-7602(NDC:49483-603)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN600 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeCAPSULESize18mm
    FlavorImprint Code 122
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68788-7602-414 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    2NDC:68788-7602-220 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    3NDC:68788-7602-721 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    4NDC:68788-7602-330 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    5NDC:68788-7602-550 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    6NDC:68788-7602-660 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    7NDC:68788-7602-990 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    8NDC:68788-7602-1100 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    9NDC:68788-7602-8120 in 1 BOTTLE; Type 0: Not a Combination Product02/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09079602/14/2020
    Labeler - Preferred Pharmaceuticals Inc. (791119022)
    Registrant - Preferred Pharmaceuticals Inc. (791119022)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preferred Pharmaceuticals Inc.791119022REPACK(68788-7602)