Active Ingredient (In Each Tablet)
Famotidine USP, 10 mg/20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Ascent Pharmaceuticals, Inc. for the product Famotidine (NDC 43602-511). 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, directions, 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
For Famotidine 10 mg:
For Famotidine 20 mg:
Hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, silicon dioxide, talc, and titanium dioxide
Please call Ascent Pharmaceuticals, Inc. at 1-855-221-1622 (toll-free number)
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