Dexmethylphenidate Hydrochloride Capsule, Extended Release
Product Images NDC 63629-2171

3 FDA label images from Bryant Ranch Prepack · 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 63629-2171). 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 diagram of Dexmethylphenidate Hydrochloride showing its molecular framework, including aromatic and cyclohexyl rings, and functional groups.*
FDA Label Image

This Is Figure 1 (Dexmethylphenidate Hydrochloride Extended Release 2)

This Is Figure 1 (Dexmethylphenidate Hydrochloride Extended Release  2)
A pharmacokinetic curve comparing dexmethylphenidate hydrochloride concentrations in ng/mL over 24 hours. It displays two lines: one for Dexmethylphenidate HCl ER 20 mg and one for Dexmethylphenidate HCl IR 2 x 10 mg, showing concentration changes over time in hours.*
FDA Label Image

Label (Lbl636292171)

Label (Lbl636292171)
Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 10 mg strength. The label includes the FDA NDC number 63629-2171-1 and states the product is prescription only. It is manufactured by Par Pharmaceutical and relabeled by Bryant Ranch Prepack. The package count is 100 capsules. Storage instructions and safety warnings about keeping medication out of reach of children 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.