Alendronate Sodium Tablet
Product Images NDC 50090-3126

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Alendronate Sodium (NDC 50090-3126). 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

Figure 1 (Alendronate Fig1)

FDA Label Image

Figure 2 (Alendronate Fig2)

Figure 2 (Alendronate Fig2)
This is a table showing the increase in bone mineral density (BMD) in postmenopausal women with osteoporosis after three years of treatment with Alendronate 10 mg/day. The BMD increase is listed as a mean percentage increase relative to placebo and is shown for three different areas of the body: the lumbar spine, femoral neck, and trochanter. The table also includes reference numbers, but they are not readable due to errors.*
FDA Label Image

Figure 3 (Alendronate Fig3)

Figure 3 (Alendronate Fig3)
Description: This appears to be a graph from a study on Osteoporosis treatment in postmenopausal women. The graph compares the effect of alendronate 10mg/day versus a placebo on Lumbar Spine BMD Percent Change From Baseline over a period of 36 months. However, the information provided is limited and difficult to interpret without further context.*
FDA Label Image

Figure 4 (Alendronate Fig4)

FDA Label Image

Studies In Glucocorticoid (Treated Patients Increase in BMD Alendronate 5 mg/day at One Year)

FDA Label Image

Studies In Paget's Disease Of Bone Effect On Serum Alkaline Phosphatase Of Alendronate 40 mg/day Versus Placebo Or Etidronate 400 mg/day (Alendronate Fig6)

Studies In Paget's Disease Of Bone Effect On Serum Alkaline Phosphatase Of Alendronate 40 mg/day Versus Placebo Or Etidronate 400 mg/day (Alendronate Fig6)
This document presents the effect of Alendronate 40 mg/day on serum alkaline phosphatase in patients with Paget's Disease of Bone in comparison to Placebo or Etidronate 400 mg/day, based on multinational and U.S. studies. It includes a graph showing the mean % change from baseline over a period of 6 months.*
FDA Label Image

Chemical Structure (Alendronate Str)

FDA Label Image

Label Image (Lbl500903126)

* 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.