Active Ingredient (In Each Tablet)
Famotidine USP, 10 mg/20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Consortium, Llc for the product Famotidine (NDC 68016-800). 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, do not use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Famotidine USP, 10 mg/20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch, synthetic red iron oxide (only in 10 mg), talc and titanium dioxide
call 1-888-375-3784
* Please review the disclaimer below.