Acyclovir Tablet
Product Images NDC 63629-9174

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acyclovir (NDC 63629-9174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Acyclovir Structure (Acyclovir 01)

Acyclovir Structure (Acyclovir 01)
Chemical structure of acyclovir showing its molecular framework with nitrogen, oxygen, and carbon atoms, including a hydroxyl-containing side chain.*
FDA Label Image

Acyclovir-02 (Acyclovir 02)

Acyclovir-02 (Acyclovir 02)
Acyclovir 800 mg oral tablet blister packaging by Bryant Ranch Prepack. The foil blister shows tablets arranged in a single row. The label includes the proprietary name acyclovir and strength 800 mg, suitable for prescription use.*
FDA Label Image

Acyclovir-03 (Acyclovir 03)

Acyclovir-03 (Acyclovir 03)
A rectangular carton for acyclovir 800 mg oral tablets by Bryant Ranch Prepack. The front panel shows the product name "acyclovir" prominently, with the strength "800 mg" and dosage form "tablet." It indicates the package contains 1 tablet. The label is primarily white and blue with black text.*
FDA Label Image

Label (Lbl636299174)

Label (Lbl636299174)
Label for Acyclovir Tablets, USP 800 mg oral tablets, repackaged by Bryant Ranch Prepack Inc., Burbank, CA. The label includes the NDC 63629-9174-1, a barcode, storage instructions, and a pack size of 50 tablets. The label displays the BRP Pharmaceuticals logo and indicates the product is Rx only.*

* 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.