Amantadine Hydrochloride
Product Images NDC 17856-0093

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 Amantadine Hydrochloride (NDC 17856-0093). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

17856 0093 30

17856 0093 30
This is a description of a medication containing Amantadine Hydrochloride, which is provided in the form of a solution. The package includes instructions for the correct dosage schedule and indications. The medication should be stored at a temperature between 20°C to 25°C and kept out of children's reach. There are additional details for the GTIN and SIN numbers, the expiration date, lot number, and the distributor's information. Customers may call a specific phone number to reorder this medication.*
FDA Label Image

17856 0093cup Label

17856 0093cup Label
These are details of two different batches of Amantadine HCL oral solution. The first batch delivers 10ml and contains 100mg/10ml of USP. It is manufactured by MGP with lot# UV1116 and packaged by UDS in Morrisville, NC 27560. It has an expiry date of 05/20/2020 and is distributed by Atlantic Biologicals Corp. The second batch delivers 5ml, is non-prescription, and has no TR number. It is manufactured by MGP with lot# UU1218 and packaged by UDS in Morrisville, NC 27560. It also has an expiry date of 05/20/2020 and is distributed by Atlantic Biologicals Corp.*
FDA Label Image

Chemical Structure (Amantadine 01)

* 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.