Carbidopa Tablet
Product Images NDC 43386-980

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbidopa (NDC 43386-980). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals,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 (7b3079e3 D9db 41aa 886f A9f95a828437 01)

Chemical structure of the active ingredient Carbidopa, showing its molecular arrangement including hydroxyl groups, methyl group, carboxyl, and hydrazine functional groups, along with a water molecule (H2O) indicating it is a hydrate form.*

FDA Label Image

30 Ct (7b3079e3 D9db 41aa 886f A9f95a828437 02)

Label for Carbidopa Tablets 25 mg, oral dosage form, prescription drug. The label indicates 30 tablets per container and is labeled by Lupin Pharmaceuticals, Inc. The NDC number 43386-980-03 is visible along with storage instructions and usage notes.*

FDA Label Image

100 Ct (7b3079e3 D9db 41aa 886f A9f95a828437 03)

Carbidopa Tablets 25 mg oral tablets label. The packaging shows 100 tablets per container, labeled for prescription use only by Lupin Pharmaceuticals, Inc. The label includes storage instructions and manufacturing information by Novel Laboratories, Inc. It also mentions use with Sinemet (Carbidopa-Levodopa) for Parkinson's disease.*

FDA Label Image

1000 Ct (7b3079e3 D9db 41aa 886f A9f95a828437 04)

Label for Carbidopa Tablets 25 mg, an oral tablet prescription drug by Lupin Pharmaceuticals, Inc. The label shows a package size of 1000 tablets and includes storage instructions and manufacturer details, stating it is manufactured by Novel Laboratories, Inc. for Lupin Pharmaceuticals.*

* 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.