How to Source Clorzoxazone + Paracetamol for Pharmaceutical Formulation
Clorzoxazone + Paracetamol (Tablets, 500mg+325mg / 300mg+250mg) is classified under Analgesic. It is therapeutically aligned with reference brands such as Generic formulations marketed under different names. This guide highlights key sourcing factors buyers should consider when procuring high-quality Clorzoxazone + Paracetamol for formulation, R&D, or bulk manufacturing.
Product Overview:
Clorzoxazone combined with Paracetamol is an effective muscle relaxant and analgesic formulation used for the relief of muscle spasms and associated pain. Clorzoxazone acts centrally to relax skeletal muscles, while Paracetamol provides analgesic and antipyretic effects, helping reduce pain and discomfort. This combination is commonly used for acute musculoskeletal conditions, including back pain, neck pain, and localized muscle pain.
1. Regulatory Compliance & Documentation
Ensure suppliers provide:
- ✔ Valid DMF (Drug Master File)
- ✔ COA (Certificate of Analysis) for each batch
- ✔ GMP, ISO, or ICH Q7 compliance certificates
2. Purity, Grade & Specification Matching
Clorzoxazone + Paracetamol must meet exact grade and purity for your dosage form:
- ✔ USP / EP / JP grade verification
- ✔ Particle size distribution check
- ✔ Residual solvent and heavy metal limits
3. Supplier Reliability & Audit History
- ✔ Positive past audit reports
- ✔ Pharma client references
- ✔ Years of proven API manufacturing experience
4. Commercial Terms: Pricing, MOQ & Flexibility
- ✔ Transparent pricing
- ✔ Pilot batch MOQ flexibility
- ✔ Volume-based discounts
5. Lead Time, Inventory & Logistics
Typical lead time for Clorzoxazone + Paracetamol is 4–6 weeks.
- ✔ Emergency dispatch options
- ✔ Regional warehousing
- ✔ Special storage if needed
6. Formulation Support
- ✔ Technical datasheets
- ✔ Sample availability
- ✔ Stability study support
Conclusion
Sourcing Clorzoxazone + Paracetamol is more than procurement—it’s a strategic partnership. With its tablets form and 500mg+325mg / 300mg+250mg specification, choosing a compliant supplier ensures consistent quality and regulatory approval. Prioritize documentation, verify compatibility, and build relationships with transparent, reliable suppliers to secure long-term success.
Next Step: Get expert assistance in sourcing Clorzoxazone + Paracetamol.
Frequently Asked Questions For Sourcing of Clorzoxazone + Paracetamol
What is the typical lead time for Clorzoxazone + Paracetamol?
Lead times range from 4–6 weeks depending on supplier and region.
Is Clorzoxazone + Paracetamol available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Clorzoxazone + Paracetamol require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Clorzoxazone + Paracetamol?
Yes, a DMF is available for regulated markets upon request. It includes detailed quality, manufacturing, and stability data.
Can I request samples or a pilot batch of Clorzoxazone + Paracetamol?
Yes — pilot batches or samples can be arranged for R&D, stability studies, or formulation trials. MOQ may vary based on region and regulatory scope.
What compliance certificates are available for Clorzoxazone + Paracetamol?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Clorzoxazone + Paracetamol suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Clorzoxazone + Paracetamol be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.
Advertise on PharmaTradZ
Reach verified pharma buyers, suppliers & decision makers worldwide.
Explore Pharma Investment Opportunities
Connect with partners, startups & ventures driving the future of pharma.