Ceftriaxone Injection, Powder, For Solution
Product Images NDC 0143-9857

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ceftriaxone (NDC 0143-9857). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Ceftriaxone For Injection 1)

Chemical structure of the active ingredient Ceftriaxone, illustrating its molecular framework including sulfur, nitrogen, oxygen atoms, and associated functional groups, along with its sodium salt form and 3.5 molecules of water of hydration.*

FDA Label Image

Cef 250mg Vial (Ceftriaxone For Injection 2)

Label for Ceftriaxone Injection, USP, 250 mg per vial as a single dose vial for intravenous or intramuscular use. The label includes storage instructions before and after reconstitution and indicates protection from light. Manufacturer is Hikma Farmacêutica (Portugal), distributed by West-Ward, Eatontown, NJ.*

FDA Label Image

Cef 250mg S-p (Ceftriaxone For Injection 3)

Ceftriaxone 500 mg/vial injection powder for solution label. The vial contains ceftriaxone equivalent to 500 mg for intravenous or intramuscular use. Manufactured by Hikma Farmacêutica (Portugal), distributed by West-Ward, NJ. Label includes reconstitution instructions for IM and IV administration and storage information.*

FDA Label Image

Cef 500mg Vial (Ceftriaxone For Injection 4)

Label for Ceftriaxone 1 gram vial injection, USP, powder for solution by Hikma Pharmaceuticals USA Inc. The vial contains a single 1 gram dose equivalent to 1 gram ceftriaxone for intravenous or intramuscular use. Instructions for reconstitution and storage information are included, with the powder protected from light. Distributed by West-Ward, Eatontown, NJ.*

FDA Label Image

Cef 500mg S-p (Ceftriaxone For Injection 5)

Ceftriaxone 2 grams/vial injection powder label for solution. It indicates 2 grams equivalent to 2 grams ceftriaxone per single dose vial for intravenous or intramuscular use. The label includes reconstitution instructions, storage recommendations, and manufacturer information, Hikma Farmacêutica (Portugal), distributed by West-Ward, Eatontown, NJ. A barcode and lot/expiration fields are visible.*

FDA Label Image

Cef 1g Vial (Ceftriaxone For Injection 6)

A product label for Ceftriaxone injection powder for solution by Hikma Pharmaceuticals USA Inc. The label includes a GTIN barcode with code 00301234567896, a serial number, an expiration date placeholder (MMYYYY), and a lot number ABCDE12345. The packaging does not specify strength or dosage form details.*

FDA Label Image

Cef 1g S-p (Ceftriaxone For Injection 7)

Label for Ceftriaxone 1 g per vial injection powder for solution, USP. The label indicates the medication is for intravenous or intramuscular use, each vial containing ceftriaxone sodium powder equivalent to 1 gram of ceftriaxone. It includes NDC 0143-9857-25, storage instructions, and manufacturer information for Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Cef 2g Vial (Ceftriaxone For Injection 8)

Label for Ceftriaxone for Injection, USP, 2 g per vial, powder for solution. The label indicates equivalence to 2 grams of ceftriaxone, intended for intravenous or intramuscular use. It is a single dose vial distributed by Hikma Pharmaceuticals USA Inc. with storage instructions and preparation guidelines included on the label.*

FDA Label Image

Cef 2g S-p (Ceftriaxone For Injection 9)

Label for Ceftriaxone injection, USP, 2 g per vial powder for solution, manufactured by Hikma Pharmaceuticals USA Inc. The label indicates the product is for intravenous or intramuscular use, with 25 single-dose vials of 2 grams each. Instructions for reconstitution and storage are included, along with the NDC 0143-9856-25.*

* 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.