Ceftriaxone Sodium 250mg Injection — Dry Powder Injections
WHO-GMP Certified Commercial Pack · Product Code: AKP-043

Ceftriaxone Sodium 250mg Injection

Formulation Overview: Sterile lyophilized parenteral cephalosporin in a 250 mg strength vial tailored for paediatric dosing and targeted single-dose intramuscular or intravenous regimens. Formulated with Ceftriaxone Sodium USP / IP (eq. Ceftriaxone 250 mg) (250 mg) in Sterile Dry Powder Injection Vial dosage form under Anti-Infectives & Antibiotics, manufactured to IP / BP / USP Compendial standards and supplied in 250 mg USP Type I Glass Vial + 5 ml Sterile WFI Ampoule with complete eCTD/ACTD regulatory dossiers, Zone IVb stability, and batch CoA for African NRAs (NAFDAC, PPB, SAHPRA, TMDA, FDA Ghana) and global tenders.
Item Code (SKU)AKP-043
Therapeutic SectorAnti-Infectives & Antibiotics
Dosage FormSterile Dry Powder Injection Vial
Active IngredientCeftriaxone Sodium USP / IP (eq. Ceftriaxone 250 mg)
Strength / Purity250 mg
Clinical IndicationPaediatric lower respiratory infections, uncomplicated gonococcal infection, otitis media, and surgical prophylaxis
Specification StandardIP / BP / USP Compendial
Packaging Format250 mg USP Type I Glass Vial + 5 ml Sterile WFI Ampoule
Shelf Life24–36 Months
Storage ConditionsStore below 25°C; protect from moisture & light
Minimum Order Quantity1000 Packs
Regulatory / Analytical DocsFull eCTD / ACTD Modules 1–5 + Zone IVb Stability Available
African & Global NRA ReadinessNAFDAC (Nigeria), PPB (Kenya), SAHPRA (SA), TMDA (Tanzania), FDA Ghana, AIRP, ARP, EFDA
Stock AvailabilityIn Stock · Immediate Commercial Dispatch
Supply StatusCommercial Export Ready

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