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Pill Identifier Information of lansoprazole 15 MG Delayed Release Capsule

Drug Information

lansoprazole 15 MG Delayed Release Capsule

Imprint: w140
Shape: C48336
Color: C48328;C48329
Ingredients: lansoprazole
Size: 16.00
Score: 1
Rxtty: SY
Author: OUR FAMILY (Nash Finch Company)
Inactive Ingredients: D&C RED NO. 33 / D&C YELLOW NO. 10 / FD&C BLUE NO. 1 / FD&C RED NO. 40 / GELATIN / HYPROMELLOSES / MAGNESIUM CARBONATE / POLYETHYLENE GLYCOLS / POLYSORBATE 80 / SILICON DIOXIDE / STARCH, CORN / SUCROSE / TALC / TITANIUM DIOXIDE / METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)>

Complete Information

  • Active ingredient (in each capsule)

    Lansoprazole 15 mg

  • Purpose

    Acid reducer

  • Use

    • treats frequent heartburn (occurs 2 or more days a week)
    • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect
  • WARNINGS

    Allergy alert: Do not use if you are allergic to lansoprazole

    Do not use
    • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.

    Ask a doctor before use if you have
    • liver disease
    • had heartburn over 3 months. This may be a sign of a more serious condition.
    • heartburn with lightheadedness, sweating or dizziness
    • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
    • frequent chest pain
    • frequent wheezing, particularly with heartburn
    • unexplained weight loss
    • nausea or vomiting
    • stomach pain

    • Ask a doctor or pharmacist before use if you are taking
    • warfarin (blood-thinning medicine)
    • prescription antifungal or anti-yeast medicines
    • digoxin (heart medicine)
    • theophylline (asthma medicine)
    • tacrolimus (immune system medicine)
    • atazanavir (medicine for HIV infection)

    Stop use and ask a doctor if
    • your heartburn continues or worsens
    • you need to take this product for more than 14 days
    • you need to take more than 1 course of treatment every 4 months
    • you get diarrhea

    If pregnant or breast-feeding

    ask a health professional before use.

  • Keep out of reach of children

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    14-Day Course of Treatment

    Repeated 14-Day Courses (if needed)

  • Other information

  • Inactive ingredients

    colloidal silicon dioxide, D & C Red No. 33, D & C Yellow No. 10, FD & C Blue No. 1, FD & C Red No. 40, gelatin, hypromellose, magnesium carbonate, methacrylic acid copolymer dispersion, polyethylene glycol, polysorbate 80, sucrose, sugar spheres, talc, titanium dioxide

  • Questions or comments?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Principal Display Panel

    Compare to the active ingredient in Prevacid® 24 HR*

    *Prevacid® 24 HR is a registered trademark of Takeda Pharmaceuticals North America, Inc., and is used under license. ©2012 Novartis Consumer Health. Inc

    HEARTBURN RELIEF 24 HOURâ„¢

    Lansoprazole Delayed- Release capsules, 15 mg

    ACID REDUCER

    Sodium Free

    Product of India

    KEEP OUTER CARTON AND PACKAGE INSERT. THEY CONTAIN IMPORTANT INFORMATION.

    TAMPER-EVIDENT BOTTLE: DO NOT USE IF INNER FOIL SEAL IMPRINTED WITH “SEALED for YOUR PROTECTION” OR DARK BLUE TO BLACK GELATIN BAND AROUND THE CENTER OF EACH CAPSULE IS MISSING OR BROKEN.

  • Product Label

    Our Family

    Lansoprazole delayed release capsules 15 mg

  • INGREDIENTS AND APPEARANCE
    HEARTBURN RELIEF 24 HOUR 
    lansoprazole capsule, delayed release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70253-019(NDC:55648-140)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LANSOPRAZOLE (UNII: 0K5C5T2QPG) (LANSOPRAZOLE - UNII:0K5C5T2QPG) LANSOPRAZOLE15 mg
    Inactive Ingredients
    Ingredient NameStrength
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GELATIN (UNII: 2G86QN327L)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM CARBONATE (UNII: 0E53J927NA)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    Product Characteristics
    ColorPINK, GREENScoreno score
    ShapeCAPSULESize16mm
    FlavorImprint Code w140
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70253-019-141 in 1 CARTON
    114 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20272703/27/2013
    Labeler - OUR FAMILY (Nash Finch Company) (006962294)
    Registrant - P and L Development of New York Corporation (800014821)