How to Source Lofexidine Hydrochloride for Pharmaceutical Formulation
Lofexidine Hydrochloride (Tablets, 0.18 mg) is classified under Medical Aid. It is therapeutically aligned with reference brands such as Lucemyra (USA). This guide highlights key sourcing factors buyers should consider when procuring high-quality Lofexidine Hydrochloride for formulation, R&D, or bulk manufacturing.
Product Overview:
Lofexidine is a non-opioid medicine used to help reduce the physical symptoms of opioid withdrawal when opioids are discontinued abruptly. It works by acting on α‑2 adrenergic receptors in the central nervous system to reduce the release of norepinephrine, thereby lowering over‑activation of the sympathetic nervous system that causes many withdrawal symptoms (like cramps, muscle aches, sweating, chills, rapid heart rate, etc.)
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
Lofexidine Hydrochloride 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 Lofexidine Hydrochloride 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 Lofexidine Hydrochloride is more than procurement—it’s a strategic partnership. With its tablets form and 0.18 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 Lofexidine Hydrochloride.
Frequently Asked Questions For Sourcing of Lofexidine Hydrochloride
What is the typical lead time for Lofexidine Hydrochloride?
Lead times range from 4–6 weeks depending on supplier and region.
Is Lofexidine Hydrochloride available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Lofexidine Hydrochloride require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Lofexidine Hydrochloride?
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 Lofexidine Hydrochloride?
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 Lofexidine Hydrochloride?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Lofexidine Hydrochloride suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Lofexidine Hydrochloride be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.
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