Ceftriaxone Sodium Injection, Powder, For Solution
Product Images NDC 85766-209

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ceftriaxone Sodium (NDC 85766-209). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sportpharm 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

Chemical-structure (Ceftriaxone Vial 01)

Chemical structure of ceftriaxone sodium, depicting its molecular components including functional groups, ring systems, and sodium ions, labeled with water of hydration (3.5 H2O).*

FDA Label Image

1 (Label 1)

Multiple labels for Ceftriaxone Sodium Injection, USP 1 gram powder for solution, relabeled by Sportpharm LLC. Labels show NDCs 85766-210-10 and 85766-210-01, indicating packages of 10 and 1 single-dose vial(s) respectively. Manufactured by Sandoz Inc. Labels include usage instructions, storage conditions, barcodes, and batch/lot placeholders.*

FDA Label Image

250 (Label 250)

Two identical labels for Ceftriaxone for Injection, USP 250 mg powder for solution, relabeled for SportPharm LLC. Each label specifies the NDC (85766-208-10 and 85766-208-01), quantity (10 and 1 single-dose vial), manufacturer Sandoz Inc., and storage instructions. The labels include batch, lot, and expiration fields, drug status as prescription (RX), and QR codes for each NDC.*

FDA Label Image

500 (Label 500)

Packaging labels for Ceftriaxone Sodium injection powder for solution, USP 500 mg strength, relabeled by Sportpharm LLC. Two labels are shown: one for a quantity of 10 vials and one for a single vial. Both mention manufacturing by Sandoz Inc. and include storage instructions and regulatory information.*

* 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.