Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 16714-979

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 16714-979). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Figure1 (Figure1)

FDA Label Image

Figure2 (Figure2)

FDA Label Image

Figure3 (Figure3)

FDA Label Image

Figure4 (Figure4)

FDA Label Image

Figure5 (Figure5)

FDA Label Image

Container1 (Container1)

Container1 (Container1)
This is a medication packaging label for Esomeprazole Magnesium Delayed-Release Capsules containing 20 mg. The text suggests that the pharmacist should dispense the medication guide to each patient. The label also provides dosage instructions and storage guidelines for the medication. Contact information for Northstar Rx LLC, and M manufacturing details are also given.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
This is a medication information for Esomeprazole Magnesium Delayed-Release Capsules USP, 40 mg. The NDC code for the medication is 16714-980-02. Each capsule contains 400mg of esomeprazole. The pharmacist should dispense the medication guide to each patient. Usual adult dosage should be referred to the package insert. The medication container should be kept tightly closed and stored at a controlled room temperature. The product is manufactured by Reddy's Laboratories Ltd.*

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