Active Ingredient (In Each Tablet)
Ranitidine 75 mg (as ranitidine hydrochloride USP, 84 mg)
The following Structured Product Label (SPL) was submitted to the FDA by Amerisource Bergen for the product Ranitidine (NDC 46122-223). 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.
Ranitidine 75 mg (as ranitidine hydrochloride USP, 84 mg)
Acid reducer
Allergy alert: Do not use if you are allergic to ranitidine 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, croscarmellose sodium, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, talc, titanium dioxide
Call 1-800-406-7984
GOOD NEIGHBOR PHARMACY
†Compare to active ingredient in Zantac 75®
NDC 46122-0223-72
Regular Strength
Acid Reducer
Ranitidine Tablets, USP 75 mg
Acid Reducer
Prevents & Relieves Heartburn Associated with Acid Indigestion & Sour Stomach
60 Tablets
Distributed By AmerisourceBergen
5103697/0613
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