Dexmethylphenidate Hydrochloride Capsule, Extended Release
Product Images NDC 72162-1473

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 72162-1473). 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.

Product Images & Figures Index

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 diagram of Dexmethylphenidate Hydrochloride showing the molecular arrangement including a piperidine ring, a phenyl group, and functional groups indicated with stereochemistry.*
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 hydrochloride concentrations over 24 hours for extended-release 20 mg and immediate-release 2 x 10 mg oral capsules. The x-axis represents time in hours, and the y-axis shows dexmethylphenidate concentration in ng/mL.*
FDA Label Image

Label (Lbl721621473)

Label (Lbl721621473)
Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 10 mg, in an oral capsule dosage form. The label indicates a prescription-only product with 100 capsules per container. It is relabeled by Bryant Ranch Prepack and manufactured by Par Formulations Private Limited. Storage instructions and safety warnings are included, alongside a barcode and NDC 72162-1473-1.*

* 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.