Active Ingredient (In Each Tablet)
Famotidine USP, 10 mg
Famotidine USP, 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Marketing Association Inc. for the product Famotidine (NDC 63868-486). 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
Famotidine USP, 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
Famotidine USP, 10 mg
Famotidine USP, 20 mg
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).
Famotidine USP, 10 mg
Famotidine USP, 20 mg
Colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide red (only for Famotidine USP, 10 mg), magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, pregelatinized starch, talc, titanium dioxide
Call 1-800-406-7984
Tips for Managing Heartburn
QC QUALITY CHOICE®
NDC 63868-714-30
Compare to the active ingredient in Original Strength PEPCID®AC†
Original Strength
Acid Controller
Famotidine Tablets USP, 10 mg
Acid Reducer
Just One Tablet
Prevents & Relieves Heartburn Due to Acid Indigestion
30 Tablets
©DISTRIBUTED BY QUALITY CHOICE
5085653 R0411
QC QUALITY CHOICE®
NDC 63868-486-25
Compare to the active ingredient in Maximum Strength PEPCID®AC†
Maximum Strength
Acid Controller
Famotidine Tablets USP, 20 mg
Acid Reducer
Just One Tablet
Prevents & Relieves Heartburn Due to Acid Indigestion
25 Tablets
©DISTRIBUTED BY QUALITY CHOICE
5077509 0110
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