Lamivudine Tablet, Film Coated
Product Images NDC 31722-753

6 FDA label images from Camber Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Lamivudine (NDC 31722-753). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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

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Lamivudine1

Lamivudine1
A line graph displaying the proportions of subjects with HIV-1 RNA under 400 copies/mL over treatment time in weeks. It compares two dosing regimens of Lamivudine: 150 mg twice daily and 300 mg once daily, showing similar trends for both groups throughout 48 weeks.*
FDA Label Image

Lamivudine150mg

Lamivudine150mg
Lamivudine 150 mg film-coated tablets carton label by Camber Pharmaceuticals, Inc. The label specifies 60 tablets, prescription use only, with storage instructions at 20° to 25°C. It includes a designated unvarnish area for batch coding and manufacturer details including Camber Pharmaceuticals, Inc., and Hetero Labs Limited, India.*
FDA Label Image

Lamivudine300mg

Lamivudine300mg
Lamivudine 300 mg film coated tablets by Camber Pharmaceuticals, Inc. The label indicates 30 tablets per bottle intended for oral use. It includes storage instructions and directs users to medication guides available online. The label also provides a barcode and batch coding area.*
FDA Label Image

Lamivudinestruc

Lamivudinestruc
Chemical structure diagram of Lamivudine showing its molecular arrangement including nitrogen, oxygen, sulfur atoms, and hydroxyl groups.*

* 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.