Carbidopa And Levodopa Capsule, Extended Release
Product Images NDC 70518-4621

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbidopa And Levodopa (NDC 70518-4621). 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

Image (10c40374 C287 4608 Bd08 5bab623bbe1d 01)

Chemical structure of Carbidopa and Levodopa showing the molecular arrangement including hydroxyl groups, amine groups, and carboxyl groups, along with a water molecule component (H2O).*

FDA Label Image

Image (10c40374 C287 4608 Bd08 5bab623bbe1d 02)

Chemical structure of Carbidopa and Levodopa, showing a benzene ring with hydroxyl groups and side chains including an amino group and carboxylic acid group.*

FDA Label Image

Mm1 (Carbidopa Levodopa 48.75mg 195mg 70518 4621 00)

Label for Carbidopa and Levodopa extended-release oral capsules, 48.75 mg/195 mg strength. The box contains 50 capsules. The label shows the NDC 70518-4621-00 and indicates the product is repackaged by RemedyRepack Inc., Indiana, PA. Additional manufacturer info lists Zydus Pharm in Pennington, NJ. Storage instructions and warnings to protect from light and moisture are also visible.*

FDA Label Image

Remedy_label (Remedy Label)

Carbidopa and Levodopa Capsule Extended-Release label showing strength 48.75 mg/195 mg. The label indicates a quantity of 1 tablet with NDC 70518-4621-01, repackaged by RemedyRepack Inc. Dosage and storage instructions are partially visible, including protection from light and moisture.*

* 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.