Abacavir Tablet, Film Coated
Product Images NDC 68084-021

View Photos of 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 (NDC 68084-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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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Abacavir 300 mg film-coated oval oral tablets. One side is imprinted with "D | 88" and the other side is plain with a score line. The tablets are tan in color. Labeler is American Health Packaging.*
FDA Label Image

Image 01

Image 01
Chemical structure diagram of Abacavir including its sulfate salt form. The image depicts the molecular arrangement with a cyclopropylamine group, purine base, and hydroxymethyl group. It represents the sulfate salt variant of the active ingredient Abacavir.*
FDA Label Image

Image 02

Image 02
Abacavir 300 mg film-coated tablets label showing a 30-tablet count (3 x 10) for oral use. The label includes a NDC number 68084-021-21 and indicates the medication is prescription only. Manufactured or distributed by American Health Packaging in Columbus, Ohio, the label also instructs on dispensing the Medication Guide and Warning Card to patients.*
FDA Label Image

Image 04

Image 04
This image shows multiple identical labels for Abacavir Tablet USP 300 mg by American Health Packaging. Each label includes the product name, strength, dosage form as a film-coated tablet, a barcode with NDC 68084-021, and placeholders for expiration date and lot number. The manufacturer location is noted as Columbus, Ohio.*

* 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.