Carbidopa And Levodopa Tablet
Product Images NDC 42291-471

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbidopa And Levodopa (NDC 42291-471). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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

100ct (471 01)

100ct (471 01)
Label for Carbidopa and Levodopa Tablets, USP 10 mg/100 mg by AvKARE. The package contains 100 tablets. The label displays the NDC 42291-471-01 and indicates the product is a prescription drug (Rx Only). It includes storage instructions and manufacturer information.*
FDA Label Image

500ct (471 50)

500ct (471 50)
Packaging label for AvKARE Carbidopa and Levodopa Tablets, USP, 10 mg/100 mg strength. The label shows the product name and strength, marks it as prescription only, and indicates a bottle size of 500 tablets. It includes the NDC number 42291-471-50 and storage instructions.*
FDA Label Image

67944b5f-figure-01 (Image 1)

67944b5f-figure-01 (Image 1)
Chemical structure of the active ingredient carbidopa, showing its molecular formula including phenol and hydrazine functional groups along with water of hydration.*
FDA Label Image

67944b5f-figure-02 (Image 2)

67944b5f-figure-02 (Image 2)
Chemical structure diagram of carbidopa, showing the molecular arrangement with hydroxyl groups and an amino acid side chain, consistent with its representation as an active ingredient in carbidopa and levodopa tablets.*

* 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.