Active Ingredient (In Each Tablet)
Famotidine, USP 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Yyba Corp for the product Welmate Famotidine 20mg (NDC 73581-109). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, keep out of reach of children., if pregnant or breast-feeding, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Famotidine, USP 20 mg
Acid reducer
Allergy alert
Do not use if you are allergic to famotidine or other acid reducers
Do not use
Ask a doctor before use if you have
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
Stop use and ask a doctor if
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
ask a health professional before use.
adults and children 12 years and over:
children under 12 years:
Microcrystalline Cellulose, Pre-gelatinized Starch, Sodium Starch Glycolate, Hydroxypropyl Cellulose, Magnesium Stearate, Hypromellose, Titanium Dioxide, Triacetin, Talc, Macrogol
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