Ceftriaxone Sodium 500mg & Sulbactam Sodium 250mg Injection — Dry Powder Injections
WHO-GMP Certified Commercial Pack · Product Code: AKP-046

Ceftriaxone Sodium 500mg & Sulbactam Sodium 250mg Injection

Formulation Overview: Mid-dose sterile 2:1 ceftriaxone-sulbactam dry powder injection formulated for intermediate IM/IV escalation therapy in hospital outpatient and inpatient wards. Formulated with Ceftriaxone Sodium IP (eq. 500 mg) + Sulbactam Sodium IP (eq. 250 mg) (500 mg + 250 mg (750 mg)) in Sterile Dry Powder Injection Vial dosage form under Anti-Infectives & Antibiotics, manufactured to IP / BP / USP Compendial standards and supplied in 750 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-046
Therapeutic SectorAnti-Infectives & Antibiotics
Dosage FormSterile Dry Powder Injection Vial
Active IngredientCeftriaxone Sodium IP (eq. 500 mg) + Sulbactam Sodium IP (eq. 250 mg)
Strength / Purity500 mg + 250 mg (750 mg)
Clinical IndicationBeta-lactamase-producing respiratory infections, complicated UTIs, and gynecological sepsis
Specification StandardIP / BP / USP Compendial
Packaging Format750 mg USP Type I Glass Vial + 5 ml Sterile WFI Ampoule
Shelf Life24–36 Months
Storage ConditionsStore below 25°C; protect from 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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