Abacavir And Lamivudine Tablet, Film Coated
Product Images NDC 68180-288

4 FDA label images from Lupin Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Abacavir And Lamivudine (NDC 68180-288). 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.

Product Images & Figures Index

FDA Label Image

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Chemical structure of Abacavir sulfate, showing the molecular structure associated with the active ingredient Abacavir in the drug Abacavir and Lamivudine tablets.*
FDA Label Image

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Chemical structure of Abacavir and Lamivudine active ingredient, showing molecular bonds and functional groups typical to the compound.*
FDA Label Image

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Label for Abacavir and Lamivudine Tablets USP 600 mg/300 mg, film-coated oral tablets by Lupin Pharmaceuticals, Inc. The label shows quantity of 30 tablets, NDC 68180-288-06, manufacturer details, dosage form, and a QR code linking to the medication guide. It includes storage instructions and active ingredient amounts.*
FDA Label Image

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Packaging label for Abacavir and Lamivudine Tablets USP 600 mg/300 mg film-coated tablets. The label indicates a 30-tablet count and specifies Lupin Pharmaceuticals, Inc. as the manufacturer. The design includes dosage and storage information, barcodes, and a QR code for medication guide access. The label features green and orange accents with the Lupin logo.*

* 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.