Cefotaxime Injection
Product Images NDC 0143-9935

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cefotaxime (NDC 0143-9935). 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

Chemical Structure (Cefotaxime For Injection Pbp 1)

Chemical structure of cefotaxime depicting its molecular components including a beta-lactam ring, sulfur, and various functional groups characteristic of this antibiotic molecule.*

FDA Label Image

Ndc 0143-9935-01 Cefotaxime For Injection, Usp Pharmacy Bulk Package Not For Direct Infusion 10 Grams* Per Pharmacy Bulk Package Not To Be Dispensed As A Unit For Iv Use Only Rx Only This Pharmacy Bulk Package Is Intended For Preparing Iv Admixtures Only. See Insert For Complete Dosage Information And Proper Use Of The Container. (Cefotaxime For Injection Pbp 2)

Cefotaxime for Injection, USP, pharmacy bulk package containing 10 grams per package, labeled for intravenous use only by Hikma Pharmaceuticals USA Inc. The label warns "PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION" and includes preparation instructions, diluent amounts for different solution concentrations, storage conditions, and distributor information for West-Ward Pharmaceutical Corp., Eatontown, NJ.*

FDA Label Image

Cefotaxime For Injection Pbp 3

Label panel for Cefotaxime injection 10 g/1, showing product information including a QR code, GTIN, serial number, expiration date, and lot number. The label is from Hikma Pharmaceuticals USA Inc., associated with NDC 0143-9935.*

* 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.