Valacyclovir Hydrochloride Tablet, Film Coated
Product Images NDC 50268-789

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 Valacyclovir Hydrochloride (NDC 50268-789). 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.

Product Images & Figures Index

FDA Label Image

Label 1 (Screen Shot 2014 09 22 At 3.39.32 Pm)

Label 1 (Screen Shot 2014 09 22 At 3.39.32 Pm)
Valacyclovir Hydrochloride 500 mg film-coated tablets in a unit dose package labeled by AvPAK. The label displays the product name, strength, dosage form, quantity of 50 tablets (5 x 10), and route of administration as oral. It includes usage instructions, storage conditions, and manufacturer details with barcode and NDC 50268-788-15.*
FDA Label Image

Label 2 (Screen Shot 2014 09 22 At 3.39.48 Pm)

Label 2 (Screen Shot 2014 09 22 At 3.39.48 Pm)
Label for Valacyclovir Tablets, USP 1 gram, film-coated oral tablets by AvPAK. The package contains 50 tablets (5 x 10) in unit dose form. It includes a barcode and states the product is prescription only, with instructions to consult the patient information leaflet. The label also provides storage conditions and manufacturer details for AvKARE, Inc.*
FDA Label Image

Chemical Structure (Valacyclovir Str)

Chemical Structure (Valacyclovir Str)
Chemical structure of Valacyclovir Hydrochloride, shown with molecular components including atoms and bonds representing its chemical composition, along with the hydrochloride (HCl) part.*

* 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.