Digoxin Solution
Product Images NDC 17856-0057

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Digoxin (NDC 17856-0057). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corps, 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

Right Arrow (32fdd8c0 1ea6 4976 9f2f 6a0dd4130ac6 01)

Digoxin 0.05 mg/mL oral solution bottle label from Atlantic Biologicals Corps. The label includes the product name Digoxin, strength 0.05 mg/mL, dosage form as an oral solution, and the labeler name Atlantic Biologicals Corps. The label is primarily blue with white text and features a clear dropper bottle.*

FDA Label Image

Down Arrow (32fdd8c0 1ea6 4976 9f2f 6a0dd4130ac6 02)

Digoxin 0.05 mg/mL oral solution packaging label from Atlantic Biologicals Corps. The label includes the product name, strength, dosage form, and manufacturer information. The label is primarily white with red and black text and features a child-resistant cap on the amber solution bottle.*

FDA Label Image

Chemical Structure (32fdd8c0 1ea6 4976 9f2f 6a0dd4130ac6 03)

Chemical structure of Digoxin showing its molecular framework with multiple rings and hydroxyl groups.*

FDA Label Image

Label Image (Rspl17856 0057)

Digoxin oral solution 0.125 mg per 2.5 mL vial label includes dosage strength and volume, prescription status, alcohol content (10% v/v), distributor Atlantic Biologicals, expiration date 04/09/13, and manufacturer Roxane. The packaging indicates delivery of 2.5 mL per dose and includes lot numbers and packaging information from UDose LLC, Miami, FL.*

* 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.