Dexmethylphenidate Hydrochloride Capsule, Extended Release
Product Images NDC 0093-5045

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Dexmethylphenidate Hydrochloride (NDC 0093-5045). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Chemical Structure For Dexmethylphenidate Hydrochloride (Image 1)

Chemical structure diagram of Dexmethylphenidate Hydrochloride showing its molecular arrangement, including a piperidine ring, a phenyl group, and associated functional groups.*

FDA Label Image

Image (Image 10)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 40 mg, by Teva Pharmaceuticals USA, Inc. The label states 100 capsules per container, with standard storage instructions and dispensing guidelines. It includes the NDC 0093-5562-01, a barcode, and directions to print medication guides from the manufacturer's website.*

FDA Label Image

Figure 1 (Image 2)

A pharmacokinetic line graph comparing dexmethylphenidate hydrochloride concentration (ng/mL) over 24 hours for extended-release capsules 20 mg and immediate-release tablets 2 x 10 mg. The graph shows concentration changes over time with distinct curves for each formulation.*

FDA Label Image

Image (Image 3)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 5 mg strength, oral dosage form, containing 100 capsules. The label includes the NDC number 0093-5550-01, manufacturer Teva Pharmaceuticals USA, Inc., and instructions for pharmacists to dispense the accompanying medication guide. Storage instructions and a barcode are also present.*

FDA Label Image

Image (Image 4)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules 10 mg by Teva Pharmaceuticals USA, Inc. The label states it is a prescription oral capsule with 100 count, includes medication guide instructions, storage conditions, and a barcode on the right. The label includes dosage form, strength, and manufacturer location.*

FDA Label Image

Image (Image 5)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules 15 mg by Teva Pharmaceuticals USA, Inc. The label indicates a 100 count package, oral extended-release capsules, with directions for pharmacist dispensing and storage instructions.*

FDA Label Image

Image (Image 6)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 20 mg strength, by Teva Pharmaceuticals USA, Inc. The label indicates a package containing 100 capsules. It includes medication guide instructions, storage conditions (20° to 25°C), and a prescription-only designation. The label also features a barcode and serialization coding area.*

FDA Label Image

Image (Image 7)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules 25 mg by Teva Pharmaceuticals USA, Inc. The label includes dosage form as extended-release capsules, pack size of 100 capsules, and storage instructions. It also provides a website for medication guides and notes the product is Rx only. The label features a barcode and serialization coding area.*

FDA Label Image

Image (Image 8)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules 30 mg by Teva Pharmaceuticals USA, Inc. The label shows dosage strength (30 mg) and quantity (100 capsules). It includes storage instructions, dispensing requirements, and a web link for medication guides. The label also displays the NDC number 0093-5554-01 and manufacturing information from Parsippany, NJ.*

FDA Label Image

Image (Image 9)

Label for Dexmethylphenidate Hydrochloride Extended-Release Capsules, 35 mg strength, oral dosage form. The label indicates a package containing 100 capsules. Manufactured by Teva Pharmaceuticals USA, Inc. The label includes storage instructions, dispensing guidance, and a barcode with NDC 0093-5046-01.*

* 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.