Epzicom
Product Images NDC 54868-5600

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Epzicom (NDC 54868-5600). 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

Abacavir Sulfate Structural Formula (1eb89a52 6461 483e 9943 F753ae2b411a 01)

Chemical structure diagram of the active ingredient in EPZICOM. The image shows the molecular structure including a bicyclic purine base with a cyclopropylamine substitution and a hydroxy-methyl-substituted sugar ring, presented with the sulfate salt form indicated.*

FDA Label Image

Lamivudine Structural Formula (1eb89a52 6461 483e 9943 F753ae2b411a 02)

Chemical structure of the active ingredient in EPZICOM, showing a purine base with an amino and keto group attached to a thiophene ring sugar moiety with a hydroxyl substituent.*

FDA Label Image

Figure 1: Hypersensitivity-related Symptoms Reported With ≥10% Frequency In Clinical Trials (n = 206 Patients) (1eb89a52 6461 483e 9943 F753ae2b411a 03)

A vertical bar chart showing the percentage occurrence of various symptoms. The x-axis lists different symptoms, and the y-axis shows the percentage scale. The chart compares two groups for each symptom with adjacent bars, visually indicating different symptom rates.*

FDA Label Image

Epzicom Bottle Label (Package Label)

Label for EPZICOM, distributed by Physicians Total Care, Inc., Tulsa, OK. The label shows the product NDC 54868-5600. It includes a lot number and an expiration date (01/60), along with the manufacturer listed as GlaxoSmithKline, Research Triangle NC. A barcode is shown at the bottom.*

* 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.