Isosorbide Mononitrate
Product Images NDC 50090-4009

4 FDA label images from A-s Medication Solutions · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Isosorbide Mononitrate (NDC 50090-4009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500904009)

Label Image (Lbl500904009)
Label for Isosorbide Mononitrate 60 mg extended-release tablets by A-S Medication Solutions. The label includes storage instructions, lot number, expiration date, and packaging details. The product NDC is 50090-4009-0.*
FDA Label Image

Structural Formula

Structural Formula
Chemical structure of Isosorbide Mononitrate, showing its molecular framework with hydroxyl and nitrate functional groups attached to a bicyclic ring system.*
FDA Label Image

Table 1

Table 1
A data table presenting pharmacokinetic parameters comparing Isosorbide Mononitrate (ISMN) 60 mg and ISMN Extended-Release Tablets 60 mg and 120 mg in single-dose and multiple-dose studies. Parameters include Cmax, Tmax, AUC, half-life (t1/2), and clearance (Cl/F), with measured ranges for each.*
FDA Label Image

Table 2

Table 2
A data table titled 'Frequency and Adverse Events (Discontinued)' summarizing adverse events from three controlled North American studies of Isosorbide Mononitrate. It presents doses (Placebo, 30 mg, 60 mg, 120 mg, 240 mg), number of patients per group, and percentages of patients experiencing headache and dizziness, including values in parentheses possibly indicating values in discontinued patients.*

* 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.