10 mg 100s Label (10 mg Central Panel 12 08 16a)
Methylphenidate Hydrochloride
Product Images NDC 55466-102
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 Methylphenidate Hydrochloride (NDC 55466-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Neolpharma, 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.
20 mg 100s Label (20 mg Central Panel 12 08 16a)
5 mg 100s Label (5 mg Central Panel 12 08 16a)
This is a description of Methylphenidate Hydrochloride tablets, a medication with the National Drug Code (NDC) 58466-101-12. Each bottle contains 100 tablets of 5mg strength. The medication is manufactured by NEOLPHARMA. The pharmacist is instructed to provide each patient with the accompanying Medication Guide.*
Methyl-hcl-struct-form (Methylphenidate 01)
HCI stands for Human-Computer Interaction. It is a field of study that focuses on the design, evaluation, and implementation of interactive computing systems for human use. HCI combines concepts from computer science, psychology, and design to create user-friendly and intuitive interfaces. This field aims to improve the interaction between humans and computers, making technology more accessible, efficient, and enjoyable. HCI professionals work on various projects, including the development of software applications, websites, mobile apps, and hardware devices. By understanding how humans interact with technology, HCI experts strive to create products that meet user needs and enhance the overall user experience.*
* 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.
