Dexmethylphenidate Hydrochloride Capsule, Extended Release
Product Images NDC 0115-1709

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dexmethylphenidate Hydrochloride (NDC 0115-1709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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

32f71710-figure-01 (Dexmethylphenidate Hydrochloride Extended Release 1)

Chemical structure of dexmethylphenidate hydrochloride, showing the molecular arrangement including a piperidine ring bonded to a phenyl group and ester functional group with a hydrochloride salt representation.*

FDA Label Image

Fig 1 (Dexmethylphenidate Hydrochloride Extended Release 2)

A line graph comparing dexmethylphenidate concentration (ng/mL) in blood over time (hours) for two formulations: Dexmethylphenidate Hydrochloride Extended-Release 20 mg and Immediate-Release 2 x 10 mg. The y-axis shows drug concentration, while the x-axis shows time up to 24 hours.*

FDA Label Image

Logo (Dexmethylphenidate Hydrochloride Extended Release 3)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules 25 mg by Amneal Pharmaceuticals of New York LLC. The label states a package size of 100 capsules, prescription use only (Rx only), and includes storage instructions, pharmacist dispensing guidance, and manufacturer and distributor information. The DEA Schedule II symbol is present.*

FDA Label Image

Logo (Dexmethylphenidate Hydrochloride Extended Release 4)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 35 mg strength, supplied in a bottle of 100 capsules. The label indicates the product is Rx only, manufactured by Amneal Pharmaceuticals of New York LLC, and includes storage and dispensing instructions, a QR code, barcode, and the NDC 0115-1710-01.*

* 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.