Methylphenidate Hydrochloride Solution
Product Images NDC 67877-602

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Methylphenidate Hydrochloride (NDC 67877-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, 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

Methylphenidate-10mg (Methylphenidate 10mg)

Methylphenidate-10mg (Methylphenidate 10mg)
This is a medication label for Methylphenidate Hydrochloride Oral Solution with a concentration of 10 mg/mL. It also includes dosage instructions, storage information, and warnings for the pharmacist. The label instructs the pharmacist to provide a Medication Guide to each patient. Manufacturing and distribution information is also provided, including the NDC number and lot number. The label contains a UV varnished area and specifies a container with a resistant closure.*
FDA Label Image

Methylphenidate-5mg (Methylphenidate 5mg)

Methylphenidate-5mg (Methylphenidate 5mg)
This is a label of NDC 67877-602-91 'G Methylphenidate Hydrochloride Oral Solution. The medication comes in 1 mg dosage and is recommended to dispense with medication guide provided separately to each patient. The storage should be at a temperature between 20-25 (65" 6 77°F). The packaging should contain a resistant closure and should not be accepted if the seal or bottle opening is broken. The manufacturer is Akem Lateratorins Ltd, and it is distributed by Ascond Laboratories LLC.*
FDA Label Image

Methylphenidate-st (Methylphenidate St)

* 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.