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.
Product Images & Figures Index
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.*
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.