Lamivudine Solution
Product Images NDC 65862-055

View Photos of 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 Lamivudine (NDC 65862-055). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Figure 1. Virologic Response Through Week 48, Epv20001a,b (intent-to-treat) (Lamivudine Figure1)

Figure 1. Virologic Response Through Week 48, Epv20001a,b (intent-to-treat) (Lamivudine Figure1)
A line graph depicting the virologic response over 48 weeks in subjects treated with Lamivudine. It compares the proportion of subjects with HIV-1 RNA under 400 copies/mL between two dosing regimens: 150 mg twice daily and 300 mg once daily, showing response trends over time in weeks.*
FDA Label Image

Package Label-principal Display Panel -10 mg/ml (240 mL Bottle Label) (Lamivudine Figure2)

Package Label-principal Display Panel -10 mg/ml (240 mL Bottle Label) (Lamivudine Figure2)
Lamivudine Oral Solution USP 10 mg/mL in a 240 mL bottle, distributed by Aurobindo Pharma USA, Inc. The label includes NDC 65862-055-24, storage instructions at 20° to 25°C, and usage warnings to keep out of reach of children. Made in India by Aurobindo Pharma Limited.*
FDA Label Image

Chemical Structure (Lamivudine Structure)

Chemical Structure (Lamivudine Structure)
Chemical structure of Lamivudine, showing its molecular framework with nitrogen, oxygen, sulfur atoms, and hydroxyl functional groups consistent with the antiviral agent. The structure depicts the key bicyclic ring system and sugar moiety characteristic of Lamivudine.*

* 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.