Combivir Tablet, Film Coated
Product Images NDC 49702-202

3 FDA label images from Viiv Healthcare Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Combivir (NDC 49702-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viiv Healthcare Company, 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

Lamivudine Chemical Structure (Combivir Spl Graphic 01)

Lamivudine Chemical Structure (Combivir Spl Graphic 01)
Chemical structure diagram of the active ingredient lamivudine. The structure shows a nucleoside analog with a thiolane ring and a cytosine base, displaying functional groups including an amino group and a hydroxyl group.*
FDA Label Image

Zidovudine Chemical Structure (Combivir Spl Graphic 02)

Zidovudine Chemical Structure (Combivir Spl Graphic 02)
Chemical structure diagram of lamivudine, an active ingredient in COMBIVIR (lamivudine and zidovudine). The structure depicts the molecular arrangement with ring formations and functional groups relevant to the compound.*
FDA Label Image

Combivir 60 Count Label (Combivir Spl Graphic 03)

Combivir 60 Count Label (Combivir Spl Graphic 03)
COMBIVIR film-coated tablets containing lamivudine and zidovudine 150 mg/300 mg are shown in this medicine carton label. The package contains 60 tablets and is manufactured and labeled by ViiV Healthcare Company. The label includes a depiction of a white oblong tablet marked with "GX FC3". Additional information includes storage instructions and a caution regarding the safety seal under the cap.*

* 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.