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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Bluepoint Laboratories for the product Famotidine (NDC 68001-494). 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 other, active ingredient in (each tablet), purpose, uses, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Famotidine USP 10 mg
Acid reducer
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
taking a prescription drug. Acid reducers may interact with certain prescription drugs.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away
carnauba wax, corn starch, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, red iron oxide, sodium starch glycolate, talc and titanium dioxide.
call
1-855-274-4122
Tips for Managing Heartburn
JUST ONE TABLET prevents and relieves heartburn due to acid indigestion brought on by eating and drinking certain foods and beverages.
Do not use if carton is open or if printed foil seal under bottle cap is open or torn.
Manufactured by:
Aurobindo Pharma Limited
Unit-VII (SEZ), Mahabubnagar (Dt)-509302, India
.
For BluePoint Laboratories
Issued: 03/2021
Famotidine Tablets USP 10 mg (30 Tablets Container Carton Label)
NDC:68001-494-04
Famotidine Tablets USP 10 mg (30 Tablets Container Label)
NDC:68001-494-04
* Please review the disclaimer below.