Acyclovir Capsule
Product Images NDC 72241-028

View Photos of 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 Acyclovir (NDC 72241-028). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Modavar Pharmaceuticals Llc, 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-100pack-fig2 (Acyclovir 100pack Fig2)

Acyclovir-100pack-fig2 (Acyclovir 100pack Fig2)
Acyclovir Capsules, USP 200 mg oral dosage form packaged in a container holding 100 capsules. The label shows the NDC 72241-028-05 and indicates the manufacturer as Cadila Pharmaceuticals Ltd. in India, with the labeler Modavar Pharmaceuticals LLC in Washington, DC. Storage instructions and a barcode are also present.*
FDA Label Image

Acyclovir-500pack-fig3 (Acyclovir 500pack Fig3)

Acyclovir-500pack-fig3 (Acyclovir 500pack Fig3)
Label for Acyclovir Capsules USP 200 mg by Modavar Pharmaceuticals LLC. The label shows the product strength as 200 mg, package size of 500 capsules, and states Rx only. Manufactured by Cadila Pharmaceuticals Ltd. in India and labeled for Modavar Pharmaceuticals LLC, Washington, DC. It includes storage, dispensing, and dosage instructions along with a barcode.*
FDA Label Image

Acyclovir-stru-fig1 (Acyclovir Structure Fig1)

Acyclovir-stru-fig1 (Acyclovir Structure Fig1)
Chemical structure of acyclovir, showing the molecular arrangement with a purine base and a hydroxyethoxy side chain. This diagram represents the active ingredient acyclovir as used in the 200 mg oral capsule by Modavar Pharmaceuticals LLC.*

* 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.