Import Ceftriaxone For Injection 125mg — Buy in Bulk from Supplier in India

Ceftriaxone for injection 125 mg is a sterile, parenteral antibiotic supplied in single‑dose vials. Each vial contains exactly 125 mg of ceftriaxone sodium, prepared under aseptic conditions to meet FDA and ISO pharmaceutical standards. The product is packaged in tamper‑proof glass vials that maintain sterility until the point of use. It is marketed as a high‑purity formulation suitable for rapid reconstitution with water for injection.

Typical industry practice for this class of antibiotic includes a sterility assurance level of 10⁻⁶, ensuring that no viable microorganisms remain in the final product. The formulation is stable for up to 24 months when stored at 2‑8 °C, a standard shelf life for injectable antibiotics. The vials are designed for quick reconstitution, allowing healthcare professionals to add the appropriate volume of WFI immediately before administration. These characteristics align with global pharmacopeial requirements for injectable medicines.

Primary users are hospitals, clinics and other healthcare facilities treating severe bacterial infections such as pneumonia, urinary‑tract infections and septicemia. Trade terms can be arranged on an FOB or CIF basis, with flexible minimum order quantities and payment options including L/C and T/T, pending supplier confirmation. Prospective buyers should request the latest batch certificates and confirm storage conditions prior to shipment.

Nootan Pharmaceuticals is located at 39/44, Prabhat Road, Lane, 9, Amarchand Pungaliya Path, Pune, Maharashtra 411004, India. The company holds a voyage trust tier, indicating a verified overseas supplier, though its platform response rate is recorded as 0 % with an average response time of zero hours. This address places the firm within Pune’s established pharmaceutical manufacturing district.

The supplier specialises in the production of sterile injectable medicines, offering products such as ceftriaxone for injection. Its listings highlight compliance with FDA and ISO standards, emphasizing aseptic manufacturing processes and batch‑level quality control. No additional corporate history or client information is provided beyond these operational details.