How to Source Tramadol + Paracetamol tablets for Pharmaceutical Formulation
Tramadol + Paracetamol tablets (Oral Tablets, 37.5 mg tramadol + 325 mg paracetamol; 75 mg + 650 mg) is classified under Analgesic. It is therapeutically aligned with reference brands such as Ultracet(US); Tramacet(EU). This guide highlights key sourcing factors buyers should consider when procuring high-quality Tramadol + Paracetamol tablets for formulation, R&D, or bulk manufacturing.
Product Overview:
Tramadol + Paracetamol tablets combine tramadol’s action as a weak opioid agonist and serotonin reuptake inhibitor with paracetamol’s inhibition of prostaglandin synthesis. This dual mechanism provides effective relief from moderate to severe pain, offering rapid onset, improved analgesia, and reduced opioid dose when used responsibly under medical supervision.
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
Tramadol + Paracetamol tablets 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 Tramadol + Paracetamol tablets 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 Tramadol + Paracetamol tablets is more than procurement—it’s a strategic partnership. With its oral tablets form and 37.5 mg tramadol + 325 mg paracetamol; 75 mg + 650 mg 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 Tramadol + Paracetamol tablets.
Frequently Asked Questions For Sourcing of Tramadol + Paracetamol tablets
What is the typical lead time for Tramadol + Paracetamol tablets?
Lead times range from 4–6 weeks depending on supplier and region.
Is Tramadol + Paracetamol tablets available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Tramadol + Paracetamol tablets require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Tramadol + Paracetamol tablets?
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 Tramadol + Paracetamol tablets?
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 Tramadol + Paracetamol tablets?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Tramadol + Paracetamol tablets suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Tramadol + Paracetamol tablets be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.