Methylphenidate Hydrochloride
Product Images NDC 53014-530

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Methylphenidate Hydrochloride (NDC 53014-530). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unither Manufacturing, Llc, 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

Chemical Structure (Methylphenidate 01)

Chemical structure of Methylphenidate Hydrochloride, illustrating its molecular components and bond configurations as shown in the image.*

FDA Label Image

Principal Display Panel (5 mg Tablet Label)

Methylphenidate Hydrochloride Tablets, USP 5 mg label showing 100 tablets per package. The label includes storage instructions, a requirement for a Medication Guide with each prescription, and dispensing conditions. Manufactured for UCB, the label displays the NDC 53014-531-07 and a barcode. The labeler is Unither Manufacturing, LLC.*

FDA Label Image

Principal Display Panel (10 mg Tablet Label)

Label for Methylphenidate Hydrochloride Tablets USP 10 mg, showing a package of 100 tablets. The label includes NDC 53014-530-07, manufacturer information from Unither Manufacturing, LLC, storage instructions, and a reminder that a Medication Guide is required for every prescription dispensed.*

FDA Label Image

Principal Display Panel (20 mg Tablet Label)

Label for Methylphenidate Hydrochloride Tablets USP 20 mg, showing a container of 100 tablets. The label includes storage instructions, dispensing guidelines, a medication guide notice, and the labeler Unither Manufacturing, LLC. NDC code 53014-532-07 is visible along with a bar code.*

* 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.