Valacyclovir Hydrochloride Tablet, Film Coated
Product Images NDC 0378-4275

3 FDA label images from Mylan Pharmaceuticals Inc. · 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 0378-4275). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan 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

Valacyclovir Tablets, Usp 500 mg Bottle Label (Image 01)

Valacyclovir Tablets, Usp 500 mg Bottle Label (Image 01)
Label for Valacyclovir Tablets, USP 500 mg film-coated oral tablets by Mylan Pharmaceuticals Inc. The label includes dosage strength, NDC 0378-4275-93, quantity of 30 tablets, storage instructions, and barcode. It specifies prescription use only and mentions packaging details with lot and expiry data coding area.*
FDA Label Image

Valacyclovir Tablets, Usp 1 Gram Bottle Label (Image 02)

Valacyclovir Tablets, Usp 1 Gram Bottle Label (Image 02)
Label for Valacyclovir Tablets, USP, 1 gram film-coated oral tablets by Mylan Pharmaceuticals Inc. The label includes dosage information, storage instructions, and a barcode. It states the tablets contain 1 gram of valacyclovir equivalent to 1.112 grams of valacyclovir hydrochloride per tablet. The package contains 30 tablets and is marked Rx only.*
FDA Label Image

Image 03

Image 03
Chemical structure diagram of valacyclovir hydrochloride, showing its molecular components including the purine base, ester side chain, and hydrochloride component.*

* 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.