How to Source Trientine Tetrahydrochloride for Pharmaceutical Formulation

Trientine Tetrahydrochloride (Tablets, Capsules, 150 mg, 250 mg) is classified under Gastrointestinal Drugs. It is therapeutically aligned with reference brands such as Syprine (USA), Cuprior (EU/UK). This guide highlights key sourcing factors buyers should consider when procuring high-quality Trientine Tetrahydrochloride for formulation, R&D, or bulk manufacturing.

Product Overview: Trientine tetrahydrochloride is a chelating agent used in the management of Wilson’s disease,...

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

Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride is more than procurement—it’s a strategic partnership. With its tablets, capsules form and 150 mg, 250 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.

Frequently Asked Questions For Sourcing of Trientine Tetrahydrochloride