Label: FAMOTIDINE tablet, film coated

  • NDC Code(s): 57896-317-03, 57896-317-06
  • Packager: GERI-CARE PHARMACEUTICAL CORP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 4, 2024

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient (in each tablet)
    Famotidine, USP 10 mg
  • Purpose
    Acid reducer
  • Uses
    relieves heartburn associated with acid indigestion and sour stomach - prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and ...
  • Warnings
    Allergy alert - Do not use if you are allergic to famotidine or other acid reducers - Do not use - if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools ...
  • Directions
    adults and children 12 years and over: to - relieve symptoms, swallow 1 tablet with a glass of water. Do not chew. to - prevent symptoms, swallow 1 tablet (of 10 mg) with a ...
  • Other information
    read the directions and warnings before use - keep the carton. It contains important information. store at 20°C to 25°C (68°F to 77°F) protect from moisture
  • Inactive ingredients
    Microcrystalline Cellulose, Pre-gelatinized Starch, Sodium Starch glycolate, Hydroxypropyl Cellulose, Magnesium stearate, Hypromellose, Titanium dioxide, Triacetin, Talc, Macrogol
  • Questions or comments?
    1-800-540-3765 (toll-free)
  • Principal Display Panel
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  • INGREDIENTS AND APPEARANCE
    Product Information