Binosto
Product Images NDC 17139-400

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Binosto (NDC 17139-400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Therapeutics, 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

Alendronate Sodium 11 Description (B278a11a Alendronat Sodium Image 1)

FDA Label Image

Binosto 70mg Label (B278a11a Blister Label1)

Binosto 70mg Label (B278a11a Blister Label1)
Binosto is a prescription effervescent tablet for oral solution containing 70mg of alendronate sodium. This blister pack contains one complete week of treatment, and is only available through prescription by a healthcare provider. Binosto is manufactured for ASCEND Therapeutics in Morristown, NJ.*
FDA Label Image

Binosto 70mg Carton 4 Tablets (B278a11a Carton 041)

Binosto 70mg Carton 4 Tablets (B278a11a Carton 041)
This is a medication label for a weekly 70 mg effervescent tablet of Alendronate Sodium. It is to be stored in a controlled room temperature between 15°C to 30°C (59°F to 86°F) and protected from moisture. Each effervescent tablet contains 9137 mg of the active ingredient. The patient is advised to read the enclosed Medication Guide before use for complete dosage and administration instructions. The label also includes manufacturing information and a note addressed to the pharmacist regarding providing the medication guide to the patient.*
FDA Label Image

Figure 1 3 Yr Study (B278a11a Figure 1 Placebo 3 Year Study)

Figure 1 3 Yr Study (B278a11a Figure 1 Placebo 3 Year Study)
The provided text is a figure caption that shows the Cumulative Incidence of Hip Fractures in a three-year study of FIT for patients with Radiographic Vertebral Fracture at Baseline. The graph displays the percentage of Cumulative Incidence for two types of treatments (Placebo and Alendronate Sodium) over time in months.*
FDA Label Image

Figure 2 Osteoporosis (B278a11a Figure 2 Osteoporosis)

Figure 2 Osteoporosis (B278a11a Figure 2 Osteoporosis)
This is a figure displaying the results of osteoporosis treatment studies in postmenopausal women. It shows the increase in Bone Mineral Density (BMD) in the Lumbar Spine, Femoral Neck and Trochanter after taking Alendronate Sodium 10mg/day for three years. The results are presented as a mean percentage increase relative to the placebo, with standard error bars shown for each.*
FDA Label Image

Figure 3 Osteoporosis (B278a11a Figure 3 Osteoporosis)

Figure 3 Osteoporosis (B278a11a Figure 3 Osteoporosis)
The text describes a figure showing the results of two studies on the effect of Alendronate Sodium treatment versus placebo in postmenopausal women with osteoporosis. The results are shown as a percent change in bone mineral density from baseline over time, specifically in the lumbar spine. The figure shows data from both a US-based study and a multinational study. The x-axis of the figure represents time in months and the y-axis represents the percent change in bone mineral density.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.