Budesonide Capsule, Coated Pellets
Product Images NDC 70518-4613

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Budesonide (NDC 70518-4613). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Budesonide (1780fdb2 9492 4cec 840e 923f19561188 01)

Chemical structure diagrams showing the epimer 22R and epimer 22S forms of budesonide, the active ingredient in this human prescription drug capsule formulation. The image displays the molecular configurations of both epimers of budesonide.*

FDA Label Image

Mm1 (Budesonide Dr 3mg 70518 4613 00)

The image shows a packaged label for Budesonide DR Capsule with a strength of 3 mg. It is an oral dosage form supplied in a box containing 50 capsules. The capsules are orange and white. The label indicates that the product is repackaged by RemedyRepack Inc., Indiana, PA, and includes storage instructions and a QR code.*

FDA Label Image

Remedy_label (Remedy Label)

Label for Budesonide DR Capsule 3 mg, containing 1 coated pellet capsule in orange and white. The label shows NDC 70518-4613-01 and indicates repackaging by RemedyRepack Inc., Indiana, PA. It includes storage instructions and a QR code, noting it is an RX only medication.*

* 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.