Active Ingredient (In Each Tablet)
Ranitidine 150 mg (as ranitidine hydrochloride USP, 168 mg)
The following Structured Product Label (SPL) was submitted to the FDA by Shopko Stores Operating Co., Llc for the product Ranitidine (NDC 37012-351). 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 150 mg (as ranitidine hydrochloride USP, 168 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, talc, titanium dioxide
Call 1-800-406-7984
SHOPKO®
Compare to the Active Ingredient of Zantac 150®
Maximum Strength
Acid Reducer
Ranitidine Tablets, USP 150 mg
Acid Reducer
Prevents & Relieves: Heartburn Associated with Acid Indigestion & Sour Stomach
50 Tablets
Packaged by: Ohm Laboratories Inc.
5093015/0212
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