Carbidopa And Levodopa Tablet
Product Images NDC 0093-9701

4 FDA label images from Teva Pharmaceuticals Usa, Inc. · 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 0093-9701). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

67944b5f-figure-01 (Image 1)

67944b5f-figure-01 (Image 1)
Chemical structure of the active ingredients Carbidopa and levodopa, showing their molecular components and arrangement, including functional groups such as hydroxyl, carboxyl, and hydrazine moieties, with a water molecule indicated.*
FDA Label Image

67944b5f-figure-02 (Image 2)

67944b5f-figure-02 (Image 2)
Chemical structure of carbidopa, an active ingredient in Carbidopa and levodopa tablets. The diagram shows the molecular arrangement of atoms characteristic to carbidopa.*
FDA Label Image

Cl 10 mg/100 mg -100s (Image 3)

Cl 10 mg/100 mg -100s (Image 3)
Label for Carbidopa and Levodopa Tablets, USP 10 mg/100 mg, oral tablets, from Teva Pharmaceuticals USA, Inc. The package contains 100 tablets. The label includes product identification, NDC 0093-9701-01, usage instructions, and regulatory information. The Teva logo is visible in green on the lower right.*
FDA Label Image

Label (Image 4)

Label (Image 4)
Label for Carbidopa and Levodopa Tablets, USP, showing strength of 25 mg/100 mg. The label indicates the product is Rx only and contains 100 tablets. The labeler is Teva Pharmaceuticals USA, Inc. Additional regulatory and packaging information is visible.*

* 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.