Clindamycin

£47,500.00

Clindamycin is a premium, broad-spectrum lincosamide antibiotic API engineered for high-purity parenteral and topical formulations, meeting stringent USP/EP pharmacopoeial standards.

Competitive Advantage Spotlight
Secured through a vertically integrated supply chain with cGMP-certified facilities, we guarantee batch-to-batch consistency, full traceability, and a validated stability profile that minimizes formulation risk for large-scale pharmaceutical manufacturers.

Description

1. Product Overview

Clindamycin is a high-purity lincosamide antibiotic widely used in pharmaceutical manufacturing for systemic and topical formulations. It serves as a critical intermediate in producing oral capsules, injectables, and topical solutions, offering targeted antibacterial efficacy against a broad spectrum of Gram-positive pathogens. Strategically, Clindamycin ensures consistent supply for essential drug production, making it a key ingredient in global healthcare supply chains. Its reliability, regulatory compliance, and proven pharmacological profile position it as a high-value sourcing choice for pharmaceutical manufacturers worldwide.


2. Key Specifications & Technical Characteristics

  • Chemical Composition: Clindamycin hydrochloride (or base, per buyer specification)
  • Purity / Grade: ≥98% pharmaceutical grade
  • Physical Form: White to off-white crystalline powder
  • Solubility: Soluble in water, methanol, and ethanol
  • Particle Size: Fine powder suitable for uniform dissolution
  • Density: ~1.3 g/cm³ (bulk density)
  • Moisture Content: ≤1.0%
  • Packaging Options: 25 kg fiber drums with double-layered inner polyethylene liners or customized per client requirements
  • Shelf Life: 24 months under recommended storage conditions (cool, dry, away from light)

3. Core Industrial Applications

  • Primary Industries:
    • Pharmaceutical manufacturing
    • Veterinary medicine production
  • Operational Use Cases:
    • Production of oral capsules, tablets, and injectables
    • Formulation of topical gels, creams, and solutions
  • Performance Advantages:
    • High stability under standard manufacturing conditions
    • Superior solubility for efficient formulation
    • Consistent batch-to-batch quality reduces process variability
  • Commercial Relevance:
    • Enhances production efficiency through reliable dissolution and bioavailability
    • Supports compliance with global regulatory standards (USP, EP, JP)

4. Competitive Advantages

  • Quality Consistency: Strict GMP-compliant manufacturing ensures uniformity across batches
  • Supply Reliability: Robust production capacity secures uninterrupted supply
  • Logistics Capability: Flexible shipping options, including containerized bulk and specialized packaging
  • Price Competitiveness: Optimized production allows cost-effective bulk sourcing
  • Sustainability: Environmentally responsible production methods and waste management practices
  • Technical Support: Comprehensive documentation, including Certificates of Analysis (CoA) and regulatory compliance data

5. Commercial & Supply Information

  • Minimum Order Quantity (MOQ): 20 MT (BULK)
  • Loading Capacity: 20 MT per standard 20-foot container

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