Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 68788-8812

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 68788-8812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals Inc., 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

Esomeprazole Magnesium Dr Capsules 40mg (40mg 30counts)

Label for Esomeprazole Magnesium DR Capsules 40 mg, a delayed-release oral capsule. The label displays the brand name, strength, dosage form, and includes storage instructions. Manufacturer is Yichang Humanwell Oral Solid Dosage Plant. The label also contains barcode and bilingual dosing instruction fields in English and Spanish. Additional fields for lot, batch, expiration, and NDC numbers are present but not filled.*

FDA Label Image

Figure-2 (Figure 2)

A line graph showing the percent maintained over a 6-month period for Esomeprazole Magnesium delayed-release capsules at doses of 40 mg, 20 mg, and 10 mg, compared to a placebo. The y-axis represents percent maintained, and the x-axis represents months, illustrating the durability of effect for each dosage versus placebo over time.*

FDA Label Image

Figure-3 (Figure 3)

A line graph illustrating the percentage maintained over a 6-month period for Esomeprazole Magnesium delayed-release capsules at 10 mg and 40 mg dosages compared to placebo. The x-axis represents months, and the y-axis shows percent maintained. Data points are plotted for each month, showing higher maintenance rates with 40 mg compared to 10 mg and placebo groups.*

FDA Label Image

Figure-4 (Figure 4)

This line graph depicts the percentage of patients symptom-free over 28 days for three groups: Esomeprazole Magnesium delayed-release capsules 40 mg, 20 mg, and placebo. The x-axis shows diary days from 0 to 28, and the y-axis shows the percent of patients symptom-free from 0 to 100. Both Esomeprazole groups show a higher percentage symptom-free compared to placebo throughout the period.*

FDA Label Image

Figure-5 (Figure 5)

A line graph depicting the percent of patients symptom-free over a 28-day diary period. It compares three groups: Esomeprazole Magnesium Delayed-Release Capsules 40 mg, Esomeprazole Magnesium Delayed-Release Capsules 20 mg, and placebo. The y-axis represents the percent of patients symptom-free, and the x-axis shows diary days from 0 to 28.*

FDA Label Image

Ink1 (Ink1)

Esomeprazole Magnesium 40 mg delayed-release capsules in a blister pack. The capsules contain pink and white beads inside a clear gelatin shell. The packaging is designed for oral use and labeled by Preferred Pharmaceuticals Inc.*

FDA Label Image

Ink2 (Ink2)

Esomeprazole Magnesium 40 mg delayed-release oral capsules packaging label. The white carton box features the proprietary name prominently at the top, with the generic name below it. The label includes a large blue capsule graphic. This is a prescription drug from Preferred Pharmaceuticals Inc. The label indicates a quantity of 100 capsules.*

FDA Label Image

Ink4 (Ink4)

Esomeprazole Magnesium 40 mg delayed-release capsules packaging label from Preferred Pharmaceuticals Inc. The label displays the proprietary and generic names, dosage strength of 40 mg, dosage form as delayed-release capsules, and product NDC 68788-8812. The route of administration is oral.*

FDA Label Image

Structure (Structure)

Chemical structure of esomeprazole magnesium showing two esomeprazole molecules coordinated with magnesium ion (Mg2+) and three water molecules (3 H2O). The diagram includes aromatic rings, methoxy groups, nitrogen, sulfur, and oxygen atoms.*

* 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.