Controlled humidity manufacturing and precision powder dosing for high-instability antibiotic and pediatric dry suspensions.
Submit your product requirements. Our technical production team calculates factory pricing & minimum batch runs.
State-of-the-art manufacturing infrastructure ensuring high bioavailability, uniform active dispersion, and superior shelf stability.
Produced in strict compliance with Schedule M & WHO-GMP norms with complete in-process batch controls.
Produced in strict compliance with Schedule M & WHO-GMP norms with complete in-process batch controls.
Produced in strict compliance with Schedule M & WHO-GMP norms with complete in-process batch controls.
Produced in strict compliance with Schedule M & WHO-GMP norms with complete in-process batch controls.
Explore verified compositions readily available for immediate third-party manufacturing and private label brand launch.
| Composition / Formulation Name | Therapeutic Category | Standard Packaging | Action |
|---|---|---|---|
| Amoxicillin 200mg + Potassium Clavulanate 28.5mg Dry Syrup → | Antibiotic Pediatric | 30ml with Sterile WFI | Get Quote |
| Amoxicillin 400mg + Potassium Clavulanate 57mg Forte Dry Syrup → | Antibiotic Pediatric | 30ml with Sterile WFI | Get Quote |
| Cefixime 50mg / 5ml Oral Dry Suspension → | Cephalosporin Antibiotic | 30ml with Sterile WFI | Get Quote |
| Cefpodoxime Proxetil 50mg / 100mg Dry Syrup | Advanced Pediatric Antibiotic | 30ml / 60ml with WFI | Get Quote |
| Azithromycin 100mg / 200mg Oral Dry Suspension | Macrolide Antibiotic | 15ml / 30ml with Measuring Cup | Get Quote |
All batches are contracted and produced under stringent Schedule M, ISO 9001:2015, and GLP laboratory testing standards.
Production lines operated in partnership with leaders including Akums Drugs & Pharmaceuticals, Windlas Biotech, Biodeal Pharmaceuticals, Medicef Pharma, and Mascot Health Series.
Every batch is accompanied by an authenticated Certificate of Analysis covering HPLC Assay, Dissolution, Disintegration, Microbial Contamination, and Heavy Metal screening.
Seamless onboarding with assistance for Loan License / Third-Party Manufacturing Agreements, Form 20B/21B compliance, and Brand Trademark NOC clearance.
Clear answers regarding batch orders, regulatory compliance, packaging, and commercial terms.
Yes, our dry syrup packs can be manufactured with pharmaceutical-grade 30ml Sterile Water for Injection (WFI) ampoules packed inside the monocarton.
Our manufacturing partners utilize dedicated humidity-controlled AHU cleanrooms maintained strictly below 20% RH with triple-layer moisture barrier induction seals.
Join 200+ pharmaceutical marketing brands that rely on Riomedica Healthcare for certified contract manufacturing.
Our technical team verifies raw material availability and provides formal quotations within 4 working hours.
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