Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 0591-0605

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 0591-0605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actavis Pharma, 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 1

FDA Label Image

Image 2

Image 2
This is a label of Labetalol Hydrochloride Tablets, USP with a strength of 30mg. This medication is used to lower blood pressure. The label indicates storage conditions, and further details about its usage are available in the package insert enclosed. The manufacturer of this product is Actavis.*
FDA Label Image

Image 3

Image 3
This is a product label for Labetalol Hydrochloride Tablets, containing 100 tablets with the National Drug Code 0591-0606.01. The tablets are manufactured by Actavis and each tablet contains Labetalol Hydrochloride. No further information about the product is available in the provided text.*
FDA Label Image

Image 4

Image 4
This is a description of a prescription medication called Labetalol Hydrochloride, which comes in the form of tablets. The tablets are from Actavis and are labeled with the NDC code 0591-0607-01. The dosage of the tablets is 100mg and they are dispensed with a prescription. The package insert contains information about the usual dosage of the medication. The rest of the text is not legible.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.