Januvia
Product Images NDC 54868-6031

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Januvia (NDC 54868-6031). 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

Bottle Label 100 mg (100mg Package Label)

This is a medication called JAKIVIA 16046 distributed by Physicians Total Care and with NDC code 54868-5848-0. The lot number is 58400320000, and the medication appears to have an expiration date of 1/60.*

FDA Label Image

Image Of Structural Formula (228ec896 E0ca 40dc 932d Ee3b3c2ffff5 01)

FDA Label Image

Image Of Figure 1 (228ec896 E0ca 40dc 932d Ee3b3c2ffff5 02)

This appears to be a graph showing the results of a study involving various treatments for hyperglycemia (high blood sugar levels). The treatments tested include a placebo, metformin alone at different dosages, and a combination of metformin and sitagliptin. The graph shows the change in blood sugar levels over a period of 24 weeks for each treatment group. The text below the graph may be a caption explaining that the values are adjusted for prior treatment and baseline blood sugar levels.*

FDA Label Image

Image Of Figure 2 (228ec896 E0ca 40dc 932d Ee3b3c2ffff5 03)

The text describes LS mean changes from baseline for patients taking Januvia 100 mg and Glipizide. The per protocol population included patients with a mean baseline A1C of 7.5% who did not experience major protocol violations and had observations at baseline and week 52.*

FDA Label Image

Bottle Label 50 mg (50mg Package Label)

* 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.