Omeprazole And Sodium Bicarbonate
Product Images NDC 13107-115

3 FDA label images from Aurolife Pharma, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omeprazole And Sodium Bicarbonate (NDC 13107-115). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurolife Pharma, 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

Omeprazole-str (Omeprazole Rx Str)

Omeprazole-str (Omeprazole Rx Str)
Chemical structure of the active ingredient Omeprazole, illustrating its molecular composition with aromatic rings, nitrogen, sulfur, and oxygen atoms as part of its structure.*
FDA Label Image

Omeprazoleandsodbicarbonate20mg1100mg

Omeprazoleandsodbicarbonate20mg1100mg
Label for Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg, indicating 30 capsules in the package. It highlights the active ingredients with their strengths, cautions for pharmacists to dispense with accompanying medication guide, storage instructions, and a statement to keep out of reach of children. The label includes the distributor name Aurobindo Pharma USA, Inc., and the NDC 13107-115-30.*
FDA Label Image

Omeprazoleandsodbicarbonate40mg1100mg

Omeprazoleandsodbicarbonate40mg1100mg
Label for Omeprazole and Sodium Bicarbonate Capsules, 40 mg/1100 mg, by Aurolife Pharma, LLC. The label indicates prescription use only and a package count of 30 capsules. It includes instructions to dispense with an accompanying Medication Guide and storage conditions at 20° to 25°C. Distributed by Aurobindo Pharma USA, Inc., Dayton, NJ.*

* 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.