Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 70771-1164

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 70771-1164). 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

Labetalol Hydrochloride Tablets (Ff56a8ca 43a3 484a B91a C6ef13d9810a 02)

Label for Labetalol Hydrochloride Tablets, USP 100 mg film-coated oral tablets. The carton contains 30 tablets and is labeled for prescription use only. The manufacturer is Cadila Healthcare Ltd., Ahmedabad, India, with Zydus Pharmaceuticals branding. Storage and dispensing instructions are included, along with the NDC 70771-1163-3 code.*

FDA Label Image

Labetalol Hydrochloride Tablets (Ff56a8ca 43a3 484a B91a C6ef13d9810a 03)

Label for Labetalol Hydrochloride Tablets, USP 200 mg film-coated oral tablets, manufactured by Zydus Lifesciences Limited. The label indicates a package containing 30 tablets for prescription use only and includes storage instructions, dosage temperature range, and a barcode.*

FDA Label Image

Labetalol Hydrochloride Tablets (Ff56a8ca 43a3 484a B91a C6ef13d9810a 04)

Label for Labetalol Hydrochloride Tablets USP, 300 mg film-coated oral tablets, packaged in a bottle of 30 tablets. The label includes storage instructions, dosage references, and a warning to keep drugs out of children's reach. Manufactured by Zydus Lifesciences Limited, Ahmedabad, India. The NDC is 70771-1165-3.*

* 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.