Ursodiol Tablet
Product Images NDC 60687-527

4 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ursodiol (NDC 60687-527). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp52721

Ahp52721
Ursodiol 250 mg oral tablet shown from two angles on a plain background. One side is embossed with the imprint "1127". The tablet is white, oblong, and uncoated. The image corresponds to the human prescription drug labelled by American Health Packaging, NDC 60687-527.*
FDA Label Image

250 mg Ursodiol Tablet Blister (Blister)

250 mg Ursodiol Tablet Blister (Blister)
Sheet of multiple Ursodiol 250 mg tablets labels from American Health Packaging. Each label includes the product name, strength 250 mg, barcode, and space for expiry and lot numbers. Labels identify the product as oral tablets with NDC 60687-527.*
FDA Label Image

250 mg Ursodiol Tablets Carton (Carton)

250 mg Ursodiol Tablets Carton (Carton)
Ursodiol 250 mg oral tablets label from American Health Packaging. The label indicates 30 tablets (3 x 10) with NDC 60687-527-21. It includes usage and storage instructions, dosage recommendations, and warnings. The label features a green gradient design element and barcode.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Ursodiol, depicting the molecular arrangement including hydroxyl and carboxyl groups characteristic of this compound.*

* 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.