Ibsrela Tablet
Product Images NDC 73154-050

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibsrela (NDC 73154-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ardelyx, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image (Ibsrela 01)

IBSRELA 53.2 mg oral tablets packaging label by Ardelyx, Inc. The label shows the proprietary and generic names (tenapanor hydrochloride), the dosage form as tablets, and the strength of 53.2 mg. The NDC 73154-050 is displayed on the label.*

FDA Label Image

Chemical Structure (Ibsrela 02)

Chemical structure of tenapanor hydrochloride, the active ingredient in IBSRELA 53.2 mg oral tablets by Ardelyx, Inc. The structure depicts the molecular arrangement including chlorine atoms and functional groups characteristic of tenapanor hydrochloride.*

FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

IBSRELA 50 mg tablets bottle label showing the brand name, generic name tenapanor, and dosage strength. The label instructs pharmacists to dispense with the accompanying medication guide and to keep the original container with desiccant. The label states the package contains 60 tablets and includes dosing instructions and storage conditions. Distributed by Ardelyx, Inc.*

FDA Label Image

Ibsrela 04

Label for IBSRELA (tenapanor) tablets, each containing 53.2 mg active ingredient, supplied as 6 tablets per container. The label includes storage instructions, dosing guidance, and states the product is distributed by Ardelyx, Inc. in Waltham, MA. It features a barcode and professional sample notation.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.