Dexmethylphenidate Hydrochloride Capsule, Extended Release
Product Images NDC 72162-1507

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 Dexmethylphenidate Hydrochloride (NDC 72162-1507). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

This Is The Structure Image (Dexmethylphenidate Hydrochloride Extended Release 1)

This Is The Structure Image (Dexmethylphenidate Hydrochloride Extended Release  1)
Chemical structure of Dexmethylphenidate Hydrochloride showing its molecular arrangement including the piperidine ring, phenyl group, hydrochloride ion, and methyl ester functional group.*
FDA Label Image

This Is Figure 1 (Dexmethylphenidate Hydrochloride Extended Release 2)

This Is Figure 1 (Dexmethylphenidate Hydrochloride Extended Release  2)
A line graph comparing dexmethylphenidate concentrations in mg/mL over time in hours for two formulations: Dexmethylphenidate HCl ER 20 mg (extended release) and Dexmethylphenidate HCl IR 2 x 10 mg (immediate release). The graph shows concentration peaks and declines up to 24 hours, illustrating pharmacokinetic profiles.*
FDA Label Image

Label (Lbl721621507)

Label (Lbl721621507)
Label for Dexmethylphenidate Hydrochloride Extended Release Capsules, 40 mg strength. The label states a package size of 100 capsules, indicates the product is prescription-only, and is relabeled by Bryant Ranch Prepack, Inc., located in Burbank, CA. It is manufactured by Par Formulations Private Limited. Storage instructions and a barcode are also present.*

* 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.