Acyclovir Suspension
Product Images NDC 68999-803

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 68999-803). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Governmental & Specialty Rx, 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.

Product Images & Figures Index

FDA Label Image

"image Description" (Acyclovir Oral Suspension 20ml Unit Dose Cup Label)

"image Description" (Acyclovir Oral Suspension 20ml Unit Dose Cup Label)
Round label for Acyclovir oral suspension, USP, with a strength of 800 mg per 20 mL. The label states it delivers 20 mL and is manufactured by Chartwell Governmental & Specialty RX, LLC. It includes instructions to shake well before using and to protect from light, with a barcode and notes indicating institutional use only.*
FDA Label Image

"image Description" (Acyclovir Oral Suspension 5ml Unit Dose Cup Label)

"image Description" (Acyclovir Oral Suspension 5ml Unit Dose Cup Label)
A circular label for Acyclovir Oral Suspension, USP, 200 mg/5 mL. The label indicates a 5 mL dose delivery, includes the NDC number 68999-803-05, and instructions to shake well and protect from light. It is labeled as Rx only for institutional use, manufactured by Chartwell Governmental & Specialty RX, LLC, Congers, NY. The label also shows a barcode and placeholders for lot number and expiration date.*
FDA Label Image

"image Description" (Acyclovir Structure)

"image Description" (Acyclovir Structure)
Chemical structure of Acyclovir, depicting the molecular arrangement commonly associated with this antiviral medication.*

* 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.