Cefepime Injection, Powder, For Solution
Product Images NDC 60505-6245

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Cefepime (NDC 60505-6245). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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-gram-anti (Carton 1 Gram 10 Vial Pack Anti Premier)

Cefepime 1 gram/vial injection powder for solution carton by Apotex Corp. The label indicates 10 single-dose 1 gram vials for intravenous use, with instructions for reconstitution and storage. The label features dosage and handling instructions, manufacturer information, and a barcode.*

FDA Label Image

Carton-1-gram (Carton 1 Gram 10 Vial Pack Premier)

Cefepime 1 gram/vial injection powder for solution carton label. The label specifies it is for intravenous use, supplied as 10 single-dose 1 gram vials. The labeler is Apotex Corp., with manufacturing by Qilu Pharmaceutical Co., Ltd. The carton includes instructions to reconstitute before use, store at 20° to 25°C, protect from light, and retain in the carton until use.*

FDA Label Image

Carton-2-gram-anti (Carton 2 Gram 10 Vial Pack Anti Premier)

Cefepime 2 grams per vial injection powder for solution, for intravenous use, manufactured by Apotex Corp. The package contains ten 2 gram single-dose vials. Label instructions include dilution prior to infusion and storage advice to protect from light and store at 20° to 25°C. The product is labeled for Rx only and made by QiLu Antibiotics Pharmaceutical Co., Ltd., China, and manufactured for Apotex Corp., Florida, USA.*

FDA Label Image

Carton-2-gram (Carton 2 Gram 10 Vial Pack Premier)

Cefepime for Injection, USP 2 grams/vial powder for solution, packaged as 10 single-dose 2 gram vials. Label indicates dilution before intravenous infusion, storage instructions, and manufacturer information including Apotex Corp., Weston, Florida, and Qilu Pharmaceutical Co., Ltd., China.*

FDA Label Image

Cefepime-structure (Cefepime Structure)

Chemical structure diagram of Cefepime, showing its molecular components including rings, methyl groups, carboxyl group, and chloride and water components as part of the structure.*

FDA Label Image

Vial-1-gram-anti (Vial 1 Gram Anti Premier)

Label for Cefepime for Injection, USP, 1 gram per vial, a single-dose powder for solution injectable intravenously. The label indicates it is manufactured by Qilu Antibiotics Pharmaceutical Co., Ltd. for Apotex Corp. Instructions include dilution before intravenous infusion. Lot, expiration date, and barcode details appear on the right side.*

FDA Label Image

Vial-1-gram (Vial 1 Gram Premier)

Label for Cefepime for Injection, USP 1 gram per vial, a single-dose powder for solution for injection. The label indicates it is for intravenous infusion after reconstitution and dilution. It shows storage instructions, manufacturer Qilu Pharmaceutical Co., Ltd., and distribution by Apotex Corp.*

FDA Label Image

Vial-2-gram-anti (Vial 2 Gram Anti Premier)

Label for Cefepime for Injection, USP, 2 grams per vial, single-dose vial for intravenous infusion. The label includes storage instructions, manufacturer information (Qilu Antibiotics Pharmaceutical Co., Ltd.) and labeler (Apotex Corp.), barcode, and lot/expiration placeholders. The product is marketed under the PREMIERProRx brand.*

FDA Label Image

Vial-2-gram (Vial 2 Gram Premier)

Label for Cefepime for Injection, USP 2 grams/vial, a single-dose vial powder for solution by Apotex Corp. Directions indicate dilution before intravenous infusion. The label notes storage at 20° to 25°C in dry state and light protection, with manufacturing details and expiration placeholder 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.