Valacyclovir Hydrochloride
Product Images NDC 70934-387

3 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · 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 70934-387). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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 (70934 385 04 Rev A 06 19)

Label (70934 385 04   Rev A 06 19)
Valacyclovir Hydrochloride Tablets, USP 1 gram, packaged as a bottle containing 4 tablets. Label includes NDC 70934-385-04, states prescription only, storage instructions, and is labeled by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label also features a barcode and lot, expiration, and manufacturing information fields.*
FDA Label Image

Label (70934 387 14 Rev A 06 19)

Label (70934 387 14   Rev A 06 19)
Packaging label for Valacyclovir Tablets, USP 500 mg by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates a package containing 14 tablets, for prescription use only. Storage instructions specify 20°-25°C (68°-77°F) controlled room temperature. The label also includes NDC 70934-387-14 and advises keeping out of reach of children in the original container.*
FDA Label Image

Chemical Structure (Valacyclovir Str)

Chemical Structure (Valacyclovir Str)
Chemical structure diagram of Valacyclovir Hydrochloride showing the molecular arrangement of atoms including amine groups, carbonyl groups, and an isopropyl moiety attached to a central carbon, along with a 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.