Acyclovir Tablet
Product Images NDC 50268-062

3 FDA label images from Avpak · 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 Acyclovir (NDC 50268-062). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

Label (Screen Shot 2014 01 23 At 3.34.11 Pm)

Label (Screen Shot 2014 01 23 At 3.34.11 Pm)
Acyclovir Tablets USP 400 mg oral tablets with packaging showing two identical labels. Each label includes the product name, strength (400 mg), NDC number (50268-061-15), and package size (50 tablets, 5x10 unit dose). The label states Rx only and provides storage instructions, manufacturer (AvPAK, Pulaski, TN), and barcode information. The logo for AvPAK is displayed at the bottom.*
FDA Label Image

800mg Label (Screen Shot 2014 07 21 At 9.22.30 Am)

800mg Label (Screen Shot 2014 07 21 At 9.22.30 Am)
Acyclovir Tablets USP 800 mg oral tablets packaging label from AvPAK. The label indicates a quantity of 50 tablets (5 x 10) wrapped as unit dose. It includes storage instructions at 20° to 25°C and precautions to keep out of children's reach. The label also displays the NDC number 50268-062-15 and barcode.*
FDA Label Image

Structural Formula For Acyclovir (B9e8a433 621d 4b2a 9c1a Aacec9200c8a 01)

Structural Formula For Acyclovir (B9e8a433 621d 4b2a 9c1a Aacec9200c8a 01)
Chemical structure of the active ingredient Acyclovir, showing its molecular composition with nitrogen, oxygen atoms, and a hydroxyl group-containing side chain.*

* 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.