Dexmethylphenidate Hydrochloride
Product Images NDC 69189-2685

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexmethylphenidate Hydrochloride (NDC 69189-2685). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avera Mckennan Hospital, 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

Dexmethylphenidate Xr 20 mg Capsule Label (6918926851)

This is a description of a medication called Dexmethylphenidate XR manufactured by Sandoz. It is a 20 mg capsule with a manufacturing lot number of F0004 and an expiration date of 11/30/2016. The National Drug Code (NDC) for this medication is 691 8926851. It appears to have been intended for distribution to a hospital or medical facility for use in Class C-1 patients. The remaining text after the NDC number is not readable.*

FDA Label Image

Dexmethylphenidate Hydrochloride Structural Formula. (Abd467a8 0340 4f41 9eed E7701b06b114 01)

FDA Label Image

Figure 1 Mean Dexmethylphenidate Plasma Concentration-time Profiles After Administration Of 1 X 20 mg Dexmethylphenidate Hydrochloride Extended-release Capsules (n=24) And 2 X 10 mg Dexmethylphenidate Hydrochloride Immediate-release Tablets (n=25) (Abd467a8 0340 4f41 9eed E7701b06b114 02)

This is a table showing the concentration of dexmethylphenidate in ng/mL with values of 20 and 15. The table also mentions Dexmethylphenidate Hydrochloride Extended-Release Capsules 20 mg and Immediate-Release Tablets 2 x 10 mg.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.