Ceftriaxone Injection, Solution
Product Images NDC 0338-5002

7 FDA label images from Baxter Healthcare Company · 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 Ceftriaxone (NDC 0338-5002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Company, 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 Formulation For Ceftriaxone Sodium (Image 01)

Chemical Formulation For Ceftriaxone Sodium (Image 01)
Chemical structure of Ceftriaxone Sodium, showing the molecular arrangement including sodium salt and water of hydration (7.2 H2O). This structure represents the active ingredient in the injection solution form of the drug.*
FDA Label Image

Ceftriaxone 1 G Representative Container Label Ndc 0338-5002 (Image 02)

Ceftriaxone 1 G Representative Container Label Ndc 0338-5002 (Image 02)
Ceftriaxone Injection, USP (in Dextrose) 1 g/50 mL single dose vial label by Baxter Healthcare Company. The sterile, nonpyrogenic solution is iso-osmotic, intended for intravenous use. The label includes storage instructions, composition details, and a barcode for product identification.*
FDA Label Image

Ceftriaxone Representative Carton Label (1 g)

Ceftriaxone Representative Carton Label (1 g)
Drug facts panels for Baxter Ceftriaxone Injection, USP (In Dextrose) 1g strength in 50 mL single-dose containers. The panels provide storage instructions including temperature requirements, thawing warnings, and shelf-life stability after thawing, along with handling precautions. The labeler is Baxter Healthcare Corporation, Deerfield, IL.*
FDA Label Image

Ceftriaxone Representative Carton Label (1 g)

Ceftriaxone Representative Carton Label (1 g)
Label for Ceftriaxone Sodium injection solution in a GALAXY container by Baxter Healthcare Company. It contains 1 gram of ceftriaxone equivalent with 1.9 grams of dextrose, adjusted with sodium hydroxide or hydrochloric acid, in a 50 mL solution for intravenous use. Label includes usage instructions, caution information, and barcodes identifiable with the NDC 0338-5002-41 and code 2G3504.*
FDA Label Image

Ceftriaxone 2 G Container Label Ndc 0338-5003 (Image 05)

Ceftriaxone 2 G Container Label Ndc 0338-5003 (Image 05)
Ceftriaxone Injection, USP (In Dextrose) 2 g/50 mL intravenous solution by Baxter Healthcare Company. The label shows a 50 mL single-dose container with iso-osmotic sterile nonpyrogenic solution. It includes directions, storage instructions, and labeler information. NDC codes 0338-5003-41 and 0263-505 are visible.*
FDA Label Image

Ceftriaxone Representative Carton Label (2 g)

Ceftriaxone Representative Carton Label (2 g)
Ceftriaxone Injection, USP (in Dextrose) 2 g in 50 mL single-dose containers. The label indicates intravenous administration and includes storage instructions to keep at or below 25°C/77°F or under refrigeration at 5°C/41°F, with a caution not to freeze or thaw by microwave. Distributed by Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Ceftriaxone Representative Carton Label (2 g)

Ceftriaxone Representative Carton Label (2 g)
Ceftriaxone Injection, Solution label for intravenous use by Baxter Healthcare Company. It indicates Ceftriaxone Sodium equivalent to 2 g ceftriaxone with 1.2 g dextrose, adjusted with sodium hydroxide and/or hydrochloric acid, in a 50 mL solution, supplied in a GALAXY container. The label includes usage instructions and cautions for preparation and administration.*

* 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.