Valacyclovir Hydrochloride
Product Images NDC 50436-3250

3 FDA label images from Unit Dose Services · 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 50436-3250). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Structure (Structure)

Structure (Structure)
Chemical structure of valacyclovir hydrochloride showing the molecular arrangement of its atoms including a purine base linked to an amino acid ester side chain with a hydrochloride moiety.*
FDA Label Image

Label Image (Lbl504363240)

Label Image (Lbl504363240)
Label for Valacyclovir 500 mg tablet by Unit Dose Services, containing instructions for dispensing and warnings. The label notes valacyclovir hydrochloride as the active ingredient, with packaging information indicating 30 tablets per unit. Manufacturer is Jubilant Generics Ltd., Roorkee, India. The label includes lot, expiration, and NDC code placeholders, plus storage instructions and pharmacist guidance.*
FDA Label Image

Label Image (Lbl504363250)

Label Image (Lbl504363250)
Packaging label for valacyclovir hydrochloride 1 g tablets, supplied in a 30-tablet bottle. The label includes storage instructions, manufacturer information (Jubilant Generics Ltd., Roorkee, India), and regulatory details such as NDC 50436-3250-1. It is labeled as RX only and includes warnings to keep out of reach of children and to store at controlled room temperature.*

* 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.