Acyclovir Tablet
Product Images NDC 70518-2117

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acyclovir (NDC 70518-2117). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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.

FDA Label Image

Mm2 (Acyclovir 400mg 70518 2117 01)

Label for Acyclovir 400 mg oral tablets, quantity 14, repackaged by RemedyRepack Inc. The label includes dosage form, strength, quantity, repackager information, original manufacturer Camber Pharma Inc., and storage instructions. The product NDC on label is 70518-2117-01.*

FDA Label Image

Mm3 (Acyclovir 400mg 70518 2117 02)

Acyclovir 400 mg oral tablets packaging label showing a quantity of 30 tablets. The label includes NDC 70518-2117-02 and states the manufacturer as Camber Pharma, Inc., Piscataway, NJ. It is repackaged by RemedyRepack Inc., Indiana, PA. The label advises storing between 20-25°C and keeping medication out of reach of children.*

FDA Label Image

Remedy_label (Remedy Label)

Acyclovir 400 mg oral tablets label showing a quantity of 30 tablets. The label includes the NDC number 70518-2117-00, manufacturing information from Camber Pharma, Inc., and repackaging details by RemedyRepack Inc., Indiana, PA. The label also advises to keep medication out of reach of children and to see the package insert for directions.*

FDA Label Image

Structure.jpg (Structure.jpg)

Chemical structure of the active ingredient acyclovir, showing its molecular arrangement with nitrogen, oxygen atoms, and a hydroxyl group attached to an alkyl chain.*

* 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.