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Drug Facts
Distributed by:
Ohm Laboratories Inc.
1385 Livingston Avenue
North Brunswick, NJ 08902
The following Structured Product Label (SPL) was submitted to the FDA by Ohm Laboratories Inc. for the product Famotidine - Acid Controller (NDC 51660-035). 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, allergy alert, do not use, ask a doctor before use if you have, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by:
Ohm Laboratories Inc.
1385 Livingston Avenue
North Brunswick, NJ 08902
Famotidine, USP 10 mg
Acid reducer
Do not use if you are allergic to famotidine or other acid reducers
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, pregelatinized starch, talc, titanium dioxide
call 1-800-406-7984
†Compare to the active ingredient of
Original Strength Pepcid AC®
NDC 51660-035-31
ohm®
ORIGINAL STRENGTH
Acid Controller
Famotidine Tablets,
USP 10 mg
Acid Reducer
30 TABLETS
Just One Tablet
Prevents & Relieves Heartburn
Due to Acid Indigestion
* Please review the disclaimer below.