Budesonide Capsule, Coated Pellets
Product Images NDC 70518-4613

View Photos of Packaging, Regulatory Labels, and Product Appearance

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)

Budesonide (1780fdb2 9492 4cec 840e 923f19561188 01)
This is a chemical formula involving epimer 227 of budesonide and epimer 225 of budesonide. Budesonide is a corticosteroid used to treat inflammatory conditions. Epimers are stereoisomers that differ in the orientation of functional groups at a single chiral center.*
FDA Label Image

Mm1 (Budesonide Dr 3mg 70518 4613 00)

Mm1 (Budesonide Dr 3mg 70518 4613 00)
This is a description of Budesonide DR Capsules in 3 mg strength, with a quantity of 50 capsules per box. The capsules are orange and white in color, and the lot number and expiration date are not available. The capsules are manufactured by Northstar Rx LLC in Memphis, Tennessee. It is recommended to store this medication at 20-25°C (68-77°F) with excursions permitted to 15-30°C (59-86°F) and to keep it out of reach of children. Additional dosage information can be found in the insert. The capsules have been repackaged by RemedyRepack Inc. in Indiana, PA.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
This is a description of a Budesonide DR Capsule with a dosage strength of 3 mg. The capsule is orange and white in color. It is a prescription medication manufactured by Northstar Rx LLC in Memphis, Tennessee. The product was repackaged by RemedyRepack Inc. The package contains 1 capsule with NDC number 70618-4613-01. The text includes information on storage conditions and a reminder to keep the medication out of reach of children. The usual dosage instructions are to be found in the insert accompanying the product.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.