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Pill Identifier Information of Ibuprofen 200 MG Oral Tablet

Drug Information

Ibuprofen 200 MG Oral Tablet

Imprint: 115
Shape: C48348
Color: C48325
Ingredients: Ibuprofen
Size: 10.00
Score: 1
Rxtty: SCD
Author: Chain Drug Consortium LLC
Inactive Ingredients: CELLULOSE, MICROCRYSTALLINE / CROSCARMELLOSE SODIUM / STARCH, CORN / TALC / COLLOIDAL SILICON DIOXIDE / MAGNESIUM STEARATE>

Complete Information

  • ACTIVE INGREDIENT(S)

    Ibuprofen 200 mg (NSAID)*

    ·        nonsteroidal anti-inflammatory drug

  • PURPOSE

    Pain reliever / fever reducer

  • USE(S)


    • temporarily relieves minor aches and pain due to :
    • backache
    • headache
    • menstrual cramps
    • minor pain of arthritis
    • muscular aches
    • the common cold
    • toothache
    • Temporarily reduces fever
  • WARNINGS

    Allergy alerts: Ibuprofen may cause a severe allergy reaction, especially in people allergic to aspirin.

    Symptoms may include: 

    • asthma (wheezing)
    • blisters
    • facial swelling
    • hives
    • rash
    • shock
    • skin reddening

    If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning: This product contains a nonsteroidal anti-inflammatory drug (NSAID), which may cause stomach bleeding. The chance is higher if you:

    • are age 60 or older
    • have bad stomach ulcers or bleeding problems
    • take a blood thinning (anticoagulant) or steroid drug
    • take other drug containing prescription NSAID (aspirin, ibuprofen, naproxen, or others)
    • have 3 or more alcoholic drinks every day while using this product
    • the more or for a longer time than directed
  • DO NOT USE

    • if you have ever had an allergic reaction to any other pain reliever/fever reducer
    • right before or after heart surgery
  • ASK A DOCTOR BEFORE USE IF

     you have

    • problems or serious side effects from taking pain relievers or fever reducers
    • stomach problems that last or come back, such as heartburn, upset stomach, or stomach pain
    • ulcers
    • bleeding problems
    • high blood pressure
    • heart or kidney disease
    • taken a diuretics
    • reached age 60 or older
  • ASK A DOCTOR OR PHARMACIST BEFORE USE IF

    you are

  • WHEN USING THIS PRODUCT

  • STOP USE AND ASK DOCTOR IF

            These are signs of stomach bleeding.

  • PREGNANCY/BREASTFEEDING

    ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause a problems in the unborn child or complications during delivery.

  • KEEP OUT OF REACH OF CHILDREN

    In case of overdose, get medical help or contact a PoisonControlCenter right away.

  • DIRECTIONS

             

    adults and children 12 years and older
    • take 1 tablet every 4 to 6 hours while symptoms persist
    • if pain or fever does not respond to 1 tablet, 2 tablets may be used
    • do not exceed 6 tablets in 24 hours, unless directed by a doctor.
    Children under 12 years
    • ask a doctor
  • INACTIVE INGREDIENT(S)

    Colloidal silicon dioxide, Croscarmellose Sodium, Magnesium stearate, Microcrystalline sodium, Pregelatinised starch, talc.

  • STORAGE

  • PRINCIPAL DISPLAY PANEL

    Carton Label PDP

    NDC# 68016-295-01

    DYE FREE
    Ibuprofen Tablets 200 mg

    PAIN RELIEVER/FEVER REDUCER (NSAID)

    SEE NEW WARNINGS INFORMATION

    100 COATED TABLETS

    Carton label - 100 count



    Bottle Label PDP

    NDC# 68016-295-01

    DYE FREE
    Ibuprofen Tablets 200 mg

    PAIN RELIEVER/FEVER REDUCER (NSAID)

    SEE NEW WARNINGS INFORMATION

    100 COATED TABLETS

    bottle-label-100ct


    Carton Label PDP

    NDC# 68016-295-50

    DYE FREE
    Ibuprofen Tablets 200 mg

    PAIN RELIEVER/FEVER REDUCER (NSAID)

    SEE NEW WARNINGS INFORMATION

    50 COATED TABLETS
    carton label-50 ct



    Bottle Label PDP

    NDC# 68016-295-50

    DYE FREE
    Ibuprofen Tablets 200 mg

    PAIN RELIEVER/FEVER REDUCER (NSAID)

    SEE NEW WARNINGS INFORMATION

    50 COATED TABLETS

    bottle-label-50 ct

  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-295
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code 115
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68016-295-011 in 1 CARTON
    1100 in 1 BOTTLE
    2NDC:68016-295-501 in 1 CARTON
    250 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09123705/07/2013
    Labeler - Chain Drug Consortium LLC (101668460)
    Registrant - Chain Drug Consortium LLC (101668460)
    Establishment
    NameAddressID/FEIBusiness Operations
    Marksans Pharma Limited925822975MANUFACTURE(68016-295)