Omeprazole And Sodium Bicarbonate Powder, For Suspension
Product Images NDC 70954-797

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 Omeprazole And Sodium Bicarbonate (NDC 70954-797). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani 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

Carton-1 (Carton 1)

Carton-1 (Carton 1)
Omeprazole and Sodium Bicarbonate For Oral Suspension 20 mg/1,680 mg powder packaging label, presented in a foldable carton format. The label indicates it contains 30 single 20-mg dose packets. Distributed by ANI Pharmaceuticals, Inc., with usage instructions and pharmacist guidance to dispense the enclosed medication guide. The active ingredient strengths and manufacturer details are clearly shown.*
FDA Label Image

Carton-2 (Carton 2)

Carton-2 (Carton 2)
Packaging label for Omeprazole and Sodium Bicarbonate oral suspension powder, 40 mg/1,680 mg strength. The label indicates it contains 30 single 40-mg dose packets and is distributed by ANI Pharmaceuticals, Inc. Directions for use and storage instructions are included, along with a note to dispense the enclosed Medication Guide to each patient.*
FDA Label Image

Foil-1 (Foil 1)

Foil-1 (Foil 1)
Packaging label for Omeprazole and Sodium Bicarbonate oral suspension powder, strength 20 mg/1,680 mg. The label includes storage instructions, a reminder to dispense the medication guide, and directions for use. The product is distributed by ANI Pharmaceuticals, Inc., Baudetee, MN, with NDC 70954-797-10.*
FDA Label Image

Foil-2 (Foil 2)

Foil-2 (Foil 2)
Omeprazole and Sodium Bicarbonate 40 mg/1,680 mg oral suspension powder packaging label. The label includes dosing information, storage instructions, and a note to dispense the enclosed Medication Guide. Distributed by ANI Pharmaceuticals, Inc., the label also features a barcode, prescription only status, and contact information.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Omeprazole, the active ingredient in Omeprazole and Sodium Bicarbonate powder for 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.