Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 60687-461

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 60687-461). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

100 mg Blister

Labetalol Hydrochloride 100 mg film-coated tablets packaging label by American Health Packaging. The label shows the drug name, strength (100 mg), route (oral), lot number (1234567), and expiration date (02/22). The layout includes multiple identical labels oriented vertically with barcode and manufacturer information.*

FDA Label Image

100 mg Carton

Labetalol Hydrochloride tablets, USP, 100 mg strength, film-coated oral tablets. The label shows a package containing 100 tablets (10 x 10) labeled for prescription use only. Distributed by American Health Packaging, Columbus, Ohio. Storage instructions and safety warnings are included on the label.*

FDA Label Image

200 mg Labetalol HCl Tablet Blister (200 mg Labetalol HCl Tablet Blister)

Label sheet featuring multiple labels for Labetalol Hydrochloride tablets, USP in 200 mg strength. The film-coated oral tablets are labeled by American Health Packaging. Each label includes a barcode, lot number, expiration date, and the company address in Columbus, Ohio.*

FDA Label Image

200 mg Labetalol HCl Tablets Carton (200 mg Labetalol HCl Tablets Carton)

Label for Labetalol Hydrochloride 200 mg film-coated oral tablets. The label indicates a package size of 100 tablets (10 blister packs of 10 tablets each). It is marked Rx Only and distributed by American Health Packaging, Columbus, Ohio. The label includes storage instructions and a barcode.*

FDA Label Image

300 mg Labetalol HCl Tablet Blister (300 mg Labetalol HCl Tablet Blister)

Labels for Labetalol Hydrochloride 300 mg film-coated tablets by American Health Packaging. Each label displays the product name, strength (300 mg), dosage form, barcode, and space for expiration date and lot number. The labels are white with black text and include the American Health Packaging address in Columbus, Ohio.*

FDA Label Image

300 mg Labetalol HCl Tablets Carton (300 mg Labetalol HCl Tablets Carton)

Label for Labetalol Hydrochloride 300 mg film-coated tablets, USP. The package contains 100 tablets (10 x 10) for oral use. Label includes dosing strength in large font, NDC 60687-461-01, and states Rx only. Distributed by American Health Packaging, Columbus, Ohio. Storage and handling instructions are provided on the label.*

FDA Label Image

Structural Formula (Structural Formula)

Chemical structure diagram of Labetalol Hydrochloride showing the molecular components and arrangement, including the hydrochloride (HCl) component.*

FDA Label Image

B1905124 D581 79a0 E053 2a95a90aeb2f

Labetalol Hydrochloride 100 mg oral film-coated tablet, round and yellow in color, with an imprint of 'T' above a score line and '98' below the score line on one side and plain on the other side. This prescription drug is labeled by American Health Packaging.*

FDA Label Image

B1905202 18f1 F437 E053 2995a90ac9a6

Labetalol Hydrochloride 100 mg film-coated round tablet with imprint "7" above the scored line and "99" below it, intended for oral use. The tablet is white and imprinted on one side; the other side is plain. Manufactured by American Health Packaging.*

FDA Label Image

B1905735 94ea 7987 E053 2a95a90ab6fd

Labetalol Hydrochloride 800 mg round, green, film-coated tablets with '800' debossed on one side and a plain other side. Oral dosage form, manufactured by American Health Packaging.*

* 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.