Cefixime 50mg Dry Syrup (per 5ml Reconstituted Suspension) — Dry Syrup
WHO-GMP Certified Commercial Pack · Product Code: AKP-081

Cefixime 50mg Dry Syrup (per 5ml Reconstituted Suspension)

Formulation Overview: Palatable fruit-flavoured paediatric third-generation cephalosporin dry powder for oral suspension engineered for smooth homogenous reconstitution and accurate weight-based dosing. Formulated with Cefixime IP (as Trihydrate, eq. Anhydrous Cefixime 50 mg / 5 ml) (50 mg / 5 ml) in Paediatric Dry Syrup (Oral Suspension) dosage form under Anti-Infectives & Antibiotics, manufactured to IP / BP / USP Compendial standards and supplied in 30 ml Amber / HDPE Bottle with Water-Mark Arrow & Measuring Cap 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-081
Therapeutic SectorAnti-Infectives & Antibiotics
Dosage FormPaediatric Dry Syrup (Oral Suspension)
Active IngredientCefixime IP (as Trihydrate, eq. Anhydrous Cefixime 50 mg / 5 ml)
Strength / Purity50 mg / 5 ml
Clinical IndicationPaediatric enteric typhoid fever, acute otitis media, pharyngitis, tonsillitis, and pediatric UTI
Specification StandardIP / BP / USP Compendial
Packaging Format30 ml Amber / HDPE Bottle with Water-Mark Arrow & Measuring Cap
Shelf Life24–36 Months
Storage ConditionsStore dry granules below 25°C; once reconstituted, use within 7 days (14 days refrigerated)
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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