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| Product NDC Code | 69230-326 | ||||||||||||
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| Drug Name | Famotidine |
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| Type | Generic | ||||||||||||
| Pharm Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||||
| Dosage Form | TABLET, FILM COATED | ||||||||||||
| RxCUI drug identifier | 199047, 310273 |
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| Application Number | ANDA215766 | ||||||||||||
| Labeler Name | Camber Consumer Care Inc | ||||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient (in each tablet) Famotidine USP 10 mg and 20 mg
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions • adults and children 12 years and over: • to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew. 10 mg: • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 15 to 60 minutes before eating food or drinking beverages that cause heartburn 20 mg: • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 10 to 60 minutes before eating food or drinking beverages that cause heartburn • do not use more than 2 tablets in 24 hours • children under 12 years: ask a doctor
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients corn starch, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate and film coating contains carnauba wax, hydroxypropyl cellulose, hypromellose, talc, titanium dioxide; and additionally 20 mg contains iron oxide red and iron oxide yellow.
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.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 beverages
Purpose
Information about the drug product’s indications for use.Purpose Acid reducer
Spl product data elements
Usually a list of ingredients in a drug product.famotidine famotidine MICROCRYSTALLINE CELLULOSE 101 STARCH, CORN SODIUM STARCH GLYCOLATE TYPE A POTATO HYPROMELLOSE 2910 (5 MPA.S) MICROCRYSTALLINE CELLULOSE 102 MAGNESIUM STEARATE HYPROMELLOSE 2910 (15 MPA.S) HYDROXYPROPYL CELLULOSE, UNSPECIFIED TITANIUM DIOXIDE TALC CARNAUBA WAX FAMOTIDINE FAMOTIDINE T;10 famotidine famotidine MICROCRYSTALLINE CELLULOSE 101 STARCH, CORN SODIUM STARCH GLYCOLATE TYPE A POTATO HYPROMELLOSE 2910 (5 MPA.S) MICROCRYSTALLINE CELLULOSE 102 MAGNESIUM STEARATE HYPROMELLOSE 2910 (15 MPA.S) HYDROXYPROPYL CELLULOSE, UNSPECIFIED TITANIUM DIOXIDE TALC CARNAUBA WAX FERRIC OXIDE RED FERRIC OXIDE YELLOW FAMOTIDINE FAMOTIDINE LIGHT YELLOW T;11
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PRINCIPAL DISPLAY PANEL Famotidine Tablets USP 10 mg - 30s container label Famotidine Tablets USP 10 mg - 30s container carton label Famotidine Tablets USP 10 mg - 10 (1x10) blister carton label Famotidine Tablets USP 20 mg - 30s container label Famotidine Tablets USP 20 mg - 30s container carton label Famotidine Tablets USP 20 mg - 10 (1x10) blister carton label famotab10mgcontlabel30s-count famotab10mgcontlabel30scontcarton famotab10mgcontlabel100scontcarton famotab20mgcontlabel-30scount famotab20mgcontlabel-30scontcarton famotab20mgcontlabel100s-contcarton
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Other information • read the directions and warnings before use • keep the carton. It contains important information. • store at 20° to 25°C (68° to 77°F) • protect from moisture
Questions or comments? 1-866-495-1995
Ask doctor
Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.Ask a doctor before use if you have • 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 • kidney disease
Ask doctor or pharmacist
Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.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. • with other acid reducers
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if • your heartburn continues or worsens • you need to take this product for more than 14 days
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breast-feeding, ask a health professional before use.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API