Budesonide Capsule
Product Images NDC 0574-9855

4 FDA label images from Padagis Us Llc · 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 Budesonide (NDC 0574-9855). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Padagis Us Llc, 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

Chemical-structure-image-1 (Chemical Structure Image 1)

Chemical-structure-image-1 (Chemical Structure Image 1)
Chemical structure of the Epimer 22R of budesonide, showing its molecular arrangement including hydroxyl, carbonyl, and ester functional groups.*
FDA Label Image

Chemical-structure-image-2 (Chemical Structure Image 2)

Chemical-structure-image-2 (Chemical Structure Image 2)
Chemical structure of budesonide, specifically labeled as Epimer 22S of budesonide, showing its molecular configuration with multiple rings, hydroxyl groups, and side chains.*
FDA Label Image

Image 01

Image 01
A label panel showing placeholders for serialization and identification data including serial number (S/N), lot number, and expiration date (Exp). Each field includes a prompt to insert the corresponding product information.*
FDA Label Image

Image 02

Image 02
The packaging label for Budesonide Delayed-Release Capsules 3 mg by Perrigo shows a carton design with prominent text stating the product name, strength, and dosage form. It includes 'Rx Only' markings, the NDC 0574-9855-10, and a package size of 100 capsules. Storage and dosing instructions are printed on one side, noting it is a bulk package not intended for dispensing. The label features the Perrigo logo and barcode details.*

* 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.