Konvomep Kit
Product Images NDC 65628-272

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Konvomep (NDC 65628-272). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity 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

Omeprazole Structure (Image 01)

FDA Label Image

Sodium Bicarbonate Structure (Image 02)

FDA Label Image

Principal Display Panel (Diluent Label)

Principal Display Panel (Diluent Label)
This is a description of a diluent product with the NDC code 65628-271-10. It is used for reconstituting omeprazole and sodium bicarbonate for oral suspension. The diluent contains 84mg/mL of sodium bicarbonate, USP, and comes in a 300 mL bottle. The pharmacist must follow the preparation instructions in the Full Prescribing Information and store the product refrigerated at 2°C to 6°C (36°F to 46°F). The recommended dosage is not specified. This product is manufactured by Azurity in Wobor, WA 01301 Ush.*
FDA Label Image

Principal Display Panel (Konvomep Label)

Principal Display Panel (Konvomep Label)
This is a medication called omeprazole and sodium bicarbonate for oral suspension. Each liter of reconstituted suspension contains 2 mg of omeprazole and 84 mg of sodium bicarbonate. The pharmacist must add the diluent provided before dispensing. The bottle contains 0.6g of omeprazole powder, and it should be used within 30 days after reconstitution. The recommended dosage should be seen in the prescribing information, and a medication guide should be dispensed to each patient. It should be stored refrigerated between 2°C to 8°C (36°F to 46°F), and it should be discarded after the expiration date.*
FDA Label Image

Principal Display Panel (Carton Label)

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