Carvedilol Tablet, Film Coated
Product Images NDC 65841-616

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carvedilol (NDC 65841-616). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Carvedilol Tablets, 3.125 mg (Cb584d62 F378 4300 A8c1 98ac6fd62812 01)

Label for Carvedilol Tablets USP 3.125 mg, film-coated oral tablets, manufactured by Zydus Lifesciences Limited. The label indicates a package size of 100 tablets, includes the NDC number 65841-616-01, barcode, storage instructions, dosage information, and safety warnings. The label is primarily white with orange and purple highlights.*

FDA Label Image

Carvedilol Tablets, 6.25 mg (Cb584d62 F378 4300 A8c1 98ac6fd62812 02)

Carvedilol Tablets, USP 6.25 mg film-coated tablets packaging label. The label shows the product name, strength, and tablet count of 100 tablets. It includes storage instructions, warnings, and the manufacturer Zydus Lifesciences Limited, India. The label also displays a barcode and a purple-green color scheme.*

FDA Label Image

Carvedilol Tablets, 12.5 mg (Cb584d62 F378 4300 A8c1 98ac6fd62812 03)

Label for Carvedilol Tablets, USP 12.5 mg, film-coated oral tablets by Zydus Lifesciences Limited. The label shows the proprietary name, strength (12.5 mg), quantity (100 tablets), and prescription status (Rx only). It includes storage instructions and manufacturer details.*

FDA Label Image

Carvedilol Tablets,25 mg (Cb584d62 F378 4300 A8c1 98ac6fd62812 04)

Label for Carvedilol Tablets, USP 25 mg, film-coated oral tablets, manufactured by Zydus Lifesciences Limited. The label indicates a package size of 100 tablets with a National Drug Code (NDC) of 65841-619-01. The label includes storage instructions, warnings, and dosage information pointing to the package insert.*

* 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.