How to Source Salmeterol And Fluticasone Propionate for Pharmaceutical Formulation
Salmeterol And Fluticasone Propionate (Powder For Inhalation(DPI/MDI), DPI (fluticasone/salmeterol): 100/50 mcg, 250/50 mcg, 500/50 mcg; MDI (fluticasone/salmeterol): 45/21 mcg, 115/21 mcg, 230/21 mcg) is classified under Respiratory Disorder. It is therapeutically aligned with reference brands such as EU & US- DPI: Advair Diskus®, AirDuo® RespiClick® , AirDuo® Digihaler®, Seretide® DiskusAirFluSal® Forspiro; EU & US - MDI: Advair HFA® , Seretide® Evohaler, Viani®. This guide highlights key sourcing factors buyers should consider when procuring high-quality Salmeterol And Fluticasone Propionate for formulation, R&D, or bulk manufacturing.
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
Salmeterol And Fluticasone Propionate 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 Salmeterol And Fluticasone Propionate 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 Salmeterol And Fluticasone Propionate is more than procurement—it’s a strategic partnership. With its powder for inhalation(dpi/mdi) form and DPI (fluticasone/salmeterol): 100/50 mcg, 250/50 mcg, 500/50 mcg; MDI (fluticasone/salmeterol): 45/21 mcg, 115/21 mcg, 230/21 mcg 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 Salmeterol And Fluticasone Propionate
What is the typical lead time for Salmeterol And Fluticasone Propionate?
Lead times range from 4–6 weeks depending on supplier and region.
Is Salmeterol And Fluticasone Propionate available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Salmeterol And Fluticasone Propionate require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Salmeterol And Fluticasone Propionate?
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 Salmeterol And Fluticasone Propionate?
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 Salmeterol And Fluticasone Propionate?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Salmeterol And Fluticasone Propionate suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Salmeterol And Fluticasone Propionate 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.