Nexium Capsule, Delayed Release
Product Images NDC 0186-5020
Product Visual Gallery
This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Nexium (NDC 0186-5020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Astrazeneca Pharmaceuticals Lp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Figure 2 Maintenance Of Healing Rates By Month (study 117) (Image 02)
Figure 3 Maintenance Of Healing Rates By Mondy (study 178) (Image 03)
Figure 4 Percent Of Patients Symptom-free Of Heartburn By Day (study 225) (Image 04)
Figure 5 Percent Of Patients Symptom-free Of Heartburn By Day (study 226) (Image 05)
Nexium 20 mg (30 Delayed-Release Capsules)
Nexium 40 mg (30 Delayed-Release Capsules)
Image 08
Image 09
Nexium 2.5 mg (30 Single Dose Granular Packet, for Delayed-Release Oral Suspension)
Nexium 5 mg (30 Single Dose Granular Packet, for Delayed-Release Oral Suspension)
Nexium 10 mg (30 Single Dose Granular Packet, for Delayed-Release Oral Suspension)
* 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.