Label: LANSOPRAZOLE capsule, delayed release

  • NDC Code(s): 43598-109-27, 43598-109-33, 43598-109-52
  • Packager: Dr. Reddy's Laboratories Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 28, 2025

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  • Active ingredient (in each capsule)
    Lansoprazole  USP, 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 - lansoprazole may cause severe skin reactions. Symptoms may include: skin reddening - blisters - rash - If an allergic reaction ...
  • Directions
    adults 18 years of age and older - this product is to be used once a day (every 24 hours), every day for 14 days - it may take 1 to 4 days for full effect, although some people get complete relief of ...
  • Other information
    read the directions and warnings before use - keep the carton. It contains important information. store at 20 – 25°C (68° – 77° F) keep product out of high heat and humidity - protect product from ...
  • Inactive ingredients
    D&C Red 28, FD&C Blue No.1, FD&C Green 3, FD&C Red 40, gelatin, hydroxypropyl cellulose, iron oxide black, low substituted hydroxypropyl cellulose, magnesium carbonate, methacrylic acid copolymer ...
  • Questions or comments?
    call 1-888-375-3784
  • SPL UNCLASSIFIED SECTION
    Tips For Managing Heartburn - • Avoid foods or drinks that are more likely to cause heartburn, such as rich, spicy, fatty and fried foods, chocolate, caffeine, alcohol and even some acidic fruits ...
  • Principal Display Panel
    Container : 14's count
  • PRINCIPAL DISPLAY PANEL
    Container carton : 14's count
  • INGREDIENTS AND APPEARANCE
    Product Information