Lamivudine
Product Images NDC 68180-603

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lamivudine (NDC 68180-603). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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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Chemical structure of lamivudine, showing its molecular composition with nitrogen, oxygen, sulfur atoms, and a crown-like sugar moiety.*

FDA Label Image

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A line graph showing proportions of subjects with HIV-1 RNA less than 400 copies/mL over 48 weeks of treatment. Two treatment regimens are compared: Lamivudine 150 mg twice daily and Lamivudine 300 mg once daily. The vertical axis represents the proportion of subjects, and the horizontal axis shows treatment time in weeks.*

FDA Label Image

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Lamivudine Tablets USP 150 mg film-coated scored tablets label displaying the active ingredient and strength. The label indicates a package size of 60 tablets. Manufactured by Lupin Limited in India and labeled for Lupin Pharmaceuticals, Inc. Storage instructions specify controlled room temperature with allowable excursions.*

FDA Label Image

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Label for Lamivudine Tablets USP 300 mg film-coated tablets, packaged in a bottle of 30 tablets. The label is from Lupin Pharmaceuticals, Inc. and includes storage instructions to store at 25°C (77°F) with permissible excursions between 15° to 30°C (59° to 86°F). It states the product is Rx only and provides manufacturing details including Lupin Limited in Goa, India.*

* 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.