Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 68001-383

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 68001-383). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories 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

Labetalol HCl Tablets Usp 100 mg 100 Tablets Label Rev 07 22

Packaging label for Labetalol Hydrochloride Tablets, USP 100 mg film-coated oral tablets. The label shows the product name, strength, and dosage form. It includes manufacturer information for BluePoint Laboratories Inc., package quantity of 100 tablets, and instructions for storage and dispensing. The label also has a barcode and NDC number 68001-381-00.*

FDA Label Image

Labetalol HCl Tablets Usp 200 mg 100 Tablets Label Rev 07 22

Label for Labetalol Hydrochloride Tablets, USP, 200 mg film-coated oral tablets by BluePoint Laboratories Inc. The label states prescription use only and provides storage instructions at 20° to 25°C. It includes manufacturer information and packaging details for 100 tablets.*

FDA Label Image

Labetalol HCl Tablets Usp 300 mg 100 Tablets Label Rev 07 22

Labetalol Hydrochloride Tablets, USP 300 mg film-coated tablets label with package size of 100 tablets. The label shows the BluePoint Laboratories Inc. logo and directs storage at controlled room temperature (20° to 25°C). The label includes dosage form as film-coated tablets and prescription-only status, with cautions to keep tightly closed and out of reach of children.*

FDA Label Image

Labetalol Hydrochloride Tablets (E4f35d97 B2d3 4f31 9606 Fd9d85b6cf7b 01)

Chemical structure of Labetalol Hydrochloride shown, depicting the molecular arrangement of atoms including a benzene ring, hydroxyl groups, and an amide functional group combined with hydrochloride (HCl).*

FDA Label Image

Labetalol HCl 100mg 100 Count Label (Rev 12-18.JPG)

The label for Labetalol Hydrochloride Tablets, USP 100 mg film-coated oral tablets, manufactured by BluePoint Laboratories Inc. It indicates the product is prescription only, with a package size of 100 tablets. Storage instructions specify controlled room temperature (20° to 25°C). The label includes barcodes, manufacturer information, and warnings to keep out of reach of children.*

FDA Label Image

Labetalol HCl 200mg 100 Count Label (Rev 12-18.JPG)

Label for Labetalol Hydrochloride Tablets, USP 200 mg film-coated tablets by BluePoint Laboratories Inc. The label shows the NDC 68001-382-00 and indicates a package of 100 tablets. It includes storage instructions, dosage reference, and child-resistant container guidance. Manufactured by Cadila Healthcare Ltd., India for BluePoint Laboratories.*

FDA Label Image

Labetalol HCl 300mg 100 Count Label (Rev 12-18.JPG)

Label for Labetalol Hydrochloride Tablets, USP 300 mg film-coated oral tablets. The label indicates 100 tablets per container, manufactured by Cadila Healthcare Ltd. India for BluePoint Laboratories. It includes storage instructions, dosage reference, and warnings, along with barcode and NDC 68001-383-00 information.*

* 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.