Carbidopa And Levodopa Tablet, Extended Release
Product Images NDC 16729-078

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbidopa And Levodopa (NDC 16729-078). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Healthcare, 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

Carbidopa-levodopa Extended Release Tablets-anda (Carbidopa Levodopa Er 25 100 30)

Label for Carbidopa and Levodopa Extended-Release Tablets USP, containing 25 mg Carbidopa and 100 mg Levodopa per tablet. The label includes dosage and storage instructions, manufacturer details (Accord Healthcare, Inc. and Intas Pharmaceuticals Limited), and shows a package count of 30 tablets. The label also features the NDC 16729-078-10 and barcode.*

FDA Label Image

Carbidopa-levodopa Extended Release Tablets-anda (Carbidopa Levodopa Er 50 200 30)

Label for Carbidopa and Levodopa Extended-Release Tablets USP, 50 mg/200 mg strength, oral dosage form. The label shows 30 tablets per container, manufactured for Accord Healthcare, Inc. It includes usage instructions, storage conditions, and manufacturer details of Intas Pharmaceuticals Limited, India.*

FDA Label Image

Carbidopa Chemical Structure (Carbidopa Levodopa Er Carbi Str)

Chemical structure of Carbidopa, showing its molecular configuration including hydroxyl groups, carboxyl group, and hydrazine moiety, associated with one molecule of water (hydrate form).*

FDA Label Image

Levodopa Chemical Structure (Carbidopa Levodopa Er Levo Str)

Chemical structure of Carbidopa and Levodopa showing the molecular arrangement of atoms.*

* 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.