Domperidone
High-purity pharmaceutical grade Domperidone API manufactured to meet stringent USP/EP specifications for gastroprokinetic and antiemetic formulations. Our pharmaceutical grade API delivers exceptional purity and consistency for critical drug manufacturing applications.
- USP/EP Grade Quality Standards
- High Purity ≥99.0% (HPLC)
- Comprehensive Analytical Documentation
- Regulatory Compliance Support
- cGMP Manufacturing Standards
- Pharmaceutical Grade Packaging
Technical Specifications
Applications
Industry-Specific Grades
DRAVYOM offers specialized Domperidone grades tailored for specific pharmaceutical requirements, ensuring optimal performance and regulatory compliance across diverse gastroprokinetic drug manufacturing applications.
USP Grade (Pharmaceutical)
EP Grade (European Pharmacopoeia)
Research Grade
GMP Grade
Quality Standards
DRAVYOM's pharmaceutical grade Domperidone is manufactured under stringent cGMP protocols, meeting international pharmaceutical standards including USP, EP, and ICH guidelines. Our pharmaceutical-grade production ensures consistent quality and regulatory compliance.
Advanced Chemical Properties & Performance
Pharmaceutical grade Domperidone exhibits exceptional chemical properties essential for gastroprokinetic therapy applications. Its ultra-pure composition and precise molecular structure ensure reliable performance in demanding pharmaceutical formulations and research applications.
Analytical Properties
Physical Properties
Pharmaceutical Performance
Purity Specifications
Stability Properties
Performance Characteristics
Detailed performance metrics demonstrate pharmaceutical grade Domperidone superiority in gastroprokinetic applications with exceptional D2 receptor antagonism, prokinetic activity, and reproducibility across diverse therapeutic protocols.
D2 Receptor Antagonism
Selective peripheral D2 receptor blockade
Minimal CNS penetrationProkinetic Activity
Enhanced gastric motility
Accelerates gastric emptyingStability Profile
Chemical stability: Excellent under storage conditions
Maintains potency for 3 yearsThermal Stability
Melting point: 242-244°C
Stable during pharmaceutical processingBatch Reproducibility
Variation: ±0.2% between batches
Consistent therapeutic efficacyLow CNS Penetration
Minimal blood-brain barrier crossing
Reduced extrapyramidal effectsSafety Information
Prescription pharmaceutical ingredient requiring professional handling. Well-established safety profile for gastroprokinetic therapy. Handle with pharmaceutical-grade safety precautions and ensure proper GMP environmental controls. Clinical monitoring for cardiac effects and prolactin levels during therapeutic use.
Storage & Handling
Store in original containers in a cool, dry, well-ventilated area away from moisture and light. Keep containers tightly closed and maintain pharmaceutical-grade environmental controls. Use appropriate GMP handling techniques for API processing.
Chemical Mechanisms & Reaction Pathways
Domperidone exhibits antiemetic and gastroprokinetic properties through selective dopamine D2 receptor antagonism in the chemoreceptor trigger zone, enhancing gastric motility and reducing nausea.
Dopamine Antagonism
Selectively blocks dopamine D2 receptors in the gut and CTZ
Reduces nausea and vomitingGastric Motility
Enhances gastric emptying and intestinal motility
Improves gastrointestinal transitPeripheral Action
Limited blood-brain barrier penetration
Reduces central nervous system effectsProlactin Effects
May increase prolactin levels through pituitary action
Requires monitoring in clinical useRegulatory Compliance & Documentation
Comprehensive regulatory compliance ensures gastrointestinal pharmaceutical manufacturing access with complete documentation packages supporting international standards and gastroprokinetic drug development.
USP Standards
United States Pharmacopeia gastroprokinetic drug specifications
EP Monograph
European Pharmacopoeia specifications for antiemetic agents
GMP Certification
Good Manufacturing Practices for gastrointestinal pharmaceuticals
ICH Guidelines
International gastrointestinal drug development regulatory compliance
DMF Support
Drug Master File for gastroprokinetic applications
Safety Documentation
Comprehensive safety and pharmacovigilance documentation
Technical Support & Value-Added Services
DRAVYOM's gastrointestinal pharmaceutical team provides comprehensive formulation support, stability testing, and regulatory services for Domperidone therapeutic applications.
Formulation Development
- Gastroprokinetic formulation optimization
- Bioavailability enhancement
- Stability testing protocols
- Custom gastrointestinal development
Analytical Services
- API purity and potency analysis
- Gastrointestinal impurity profiling
- Pharmaceutical testing services
- Method validation support
Regulatory Support
- Gastrointestinal regulatory filing
- DMF preparation and maintenance
- International compliance guidance
- Pharmacovigilance support
Supply Solutions
- Reliable pharmaceutical supply chain
- Custom packaging solutions
- Global distribution network
- Emergency supply arrangements
Environmental Impact & Sustainability
Our Domperidone production emphasizes environmental responsibility through sustainable pharmaceutical manufacturing practices, waste minimization, and comprehensive environmental impact management.
Green Chemistry
Environmentally friendly synthesis and processing methods
Water Conservation
Advanced water treatment and recycling systems
Clean Production
Energy-efficient pharmaceutical manufacturing processes
Waste Reduction
Comprehensive pharmaceutical waste management protocols
ISO 14001
Environmental management system certified production
Sustainable Sourcing
Responsible procurement of pharmaceutical raw materials
Manufacturing Excellence & Quality Control
DRAVYOM's pharmaceutical manufacturing facility employs advanced synthesis technology and continuous monitoring systems to ensure consistent Domperidone quality and therapeutic performance.
GMP Production
Advanced pharmaceutical manufacturing in controlled clean-room environment
Multi-stage purification for pharmaceutical grade qualityQuality Testing
Comprehensive testing including assay, impurities, and stability
HPLC verification and pharmaceutical analysisQuality Systems
ISO 9001:2015 quality management with pharmaceutical compliance
Continuous improvement and pharmaceutical validationPharmaceutical Packaging
Pharmaceutical-grade containers with moisture protection
Stability protection and contamination preventionMarket Applications & Performance Data
Comprehensive pharmaceutical data demonstrating Domperidone effectiveness in gastrointestinal applications with quantified performance metrics and clinical validation data.
Pharmaceutical Formulations
Therapeutic Applications
Manufacturing Performance
DRAVYOM Competitive Advantages
Pharmaceutical Excellence
Superior pharmaceutical grade quality with consistent gastroprokinetic performance and regulatory compliance
Reliable Supply
Guaranteed availability with strategic inventory management and pharmaceutical production scheduling
Formulation Expertise
Dedicated gastrointestinal pharmaceutical development team with specialized formulation support
Regulatory Compliance
Complete pharmaceutical documentation with DMF support and international compliance
Global Standards
International pharmaceutical compliance with USP, EP, and ICH guidelines
Partnership Approach
Collaborative relationships with pharmaceutical manufacturers and custom development services