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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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each tablet)Famotidine, USP 10 mg
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PurposeAcid reducer
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Usesrelieves 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 ...
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WarningsAllergy 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 ...
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Directionsadults 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 ...
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Other informationread 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
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Inactive ingredientsMicrocrystalline Cellulose, Pre-gelatinized Starch, Sodium Starch glycolate, Hydroxypropyl Cellulose, Magnesium stearate, Hypromellose, Titanium dioxide, Triacetin, Talc, Macrogol
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Questions or comments?1-800-540-3765 (toll-free)
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INGREDIENTS AND APPEARANCEProduct Information