MedPath

Congloxime-750

Brand Name: Congloxime-750

Generic Name: Cefuroxime (as Sodium)

Active
Registration Number

DRP-8403-09

Dosage Form

Powder for Injection (IM/IV)

Issuance Date

February 6, 2024

Expiry Date

February 15, 2028

Product Information

Philippine FDA product specifications and classification details

Product Specifications

Dosage Strength750 mg
PackagingUSP Type I Colorless Glass Vial with Rubber Stopper and Blu Flip-off Seal x 15 mL + 10 mL Sterile Water for Injection as diluent / (Box of 1's)

Classification

C
Classification
Prescription Drug (Rx)
P
Pharmacologic
Antibacterial (Second Generation Cephalosporin)
A
Application
CLIDP Conversion
Philippine FDA Classification

Active Ingredients (1)

Complete list of active ingredients in this pharmaceutical product.

Cefuroxime (as Sodium)Active
Monograph: cefuroxime (as sodium)

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

Product

Company

Legal

© 2025 MedPath, Inc. All rights reserved.