Methylphenidate Hydrochloride Tablet
Product Images NDC 57664-228

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Methylphenidate Hydrochloride (NDC 57664-228). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Structure (Methylphenidate 01)

Chemical structure diagram of Methylphenidate Hydrochloride showing its molecular arrangement including a phenyl ring, ester group, piperidine ring, and hydrochloride component.*

FDA Label Image

Pdp-5mg-cranbury (Methylphenidate 02)

Label for Methylphenidate Hydrochloride Tablets USP 5 mg by Sun Pharmaceutical Industries, Inc. The bottle label indicates the strength as 5 mg oral tablets, with a quantity of 100 tablets per bottle. It includes dispensing instructions for pharmacists and storage information, along with a barcode and NDC number 57664-228-88.*

FDA Label Image

Pdp-5mg-ohm (Methylphenidate 03)

Label for Methylphenidate Hydrochloride Tablets, USP 10 mg by Sun Pharmaceutical Industries, Inc. The label includes dosage form as tablets, strength of 10 mg, quantity of 100 tablets, and dispensing instructions. It also contains storage instructions, manufacturer details, and two barcodes.*

FDA Label Image

Pdp-10mg-cranbury (Methylphenidate 04)

Label for Methylphenidate Hydrochloride Tablets USP, 20 mg, by Sun Pharmaceutical Industries, Inc. The label indicates prescription use only and a package size of 100 tablets. It includes NDC 57664-230-88, dosage instructions to dispense with medication guide, and storage details. The label features barcodes and manufacturer information.*

* 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.