Metadate Cd
Product Images NDC 54868-5397

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Metadate Cd (NDC 54868-5397). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Principal Display Panel (30 mg Capsule Label)

Metadate CD 30 mg extended-release capsules label from Physicians Total Care, Inc. The label includes the active ingredient methylphenidate hydrochloride, dosage strength of 30 mg, and a count of 30 capsules. It also displays cautionary information about federal law prohibiting dispensing without prescription, along with directions for dispensing and handling, usage instructions, and manufacturer details.*

FDA Label Image

Principal Display Panel (20 mg Capsule Label)

Metadate CD 20 mg extended-release capsules label by Physicians Total Care, Inc. The label shows 30 capsules of Methylphenidate HCL USP. It includes cautionary text about prescription dispensing, NDC number 54868-4718-0, lot number, and expiration date with storage instructions. The label has a barcode and contact information for the manufacturer.*

FDA Label Image

Principal Display Panel (10 mg Capsule Label)

Metadate CD 10 mg extended-release capsules packaging label by Physicians Total Care, Inc. The label shows the product name and strength, quantity of 30 capsules, active ingredient Methylphenidate HCl USP, and includes federal caution against dispensing without prescription. Also visible are usage instructions, storage conditions, lot number, and expiry date.*

FDA Label Image

Principal Display Panel (50 mg Capsule Label)

Label for Metadate CD, 50 mg extended-release capsules by Physicians Total Care, Inc. The label lists methylphenidate HCL, USP as the active ingredient and indicates a package size of 30 capsules. It includes federal caution against dispensing without prescription, storage instructions, lot number, expiration date, barcode, and manufacturer information.*

FDA Label Image

Chemical Structure (Metadate 01)

Chemical structure depicting the active ingredient's molecular formula, featuring a methyl ester group, a phenyl ring, and a piperidine ring with a hydrochloride (HCl) component. This structure is consistent with the active ingredient in Metadate CD.*

FDA Label Image

Figure (Metadate 02)

A line graph comparing mean methylphenidate plasma concentration (ng/mL) over time (hours) after repeated doses of immediate release (IR) and METADATE CD formulations in children with ADHD. The graph includes three lines representing 1 x 10 mg IR at 0 and 4 hours, 1 x 20 mg METADATE CD, and 2 x 20 mg METADATE CD doses, with time on the x-axis up to 9 hours and concentration on the y-axis up to 16 ng/mL.*

FDA Label Image

Figure (Metadate 03)

A bar chart comparing least squares mean change from baseline in TCGIS scores between Metadate CD capsules (n=155) and placebo (n=159). The Metadate CD bar shows a greater negative change (around -7.9) compared to the placebo bar (around -1.2), with error bars indicating variability.*

FDA Label Image

Figure (Metadate 04)

A bar graph titled 'Figure 3' showing the least squares mean change from baseline in TCGIS scores for Metadate CD capsules versus placebo during morning (AM) and afternoon (PM) groups. The vertical axis represents the mean change, with Metadate CD showing larger decreases compared to placebo. Error bars indicate the standard error of the mean for each group.*

* 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.