How to Source Salbuterol Inhalers for Pharmaceutical Formulation

Salbuterol Inhalers (Inhaler, 100 μg per inhalation, 200 μg per inhalation) is classified under Medical Aid. It is therapeutically aligned with reference brands such as Ventolin HFA, ProAir HFA, Proventil HFA(US). This guide highlights key sourcing factors buyers should consider when procuring high-quality Salbuterol Inhalers 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

Salbuterol Inhalers 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 Salbuterol Inhalers 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 Salbuterol Inhalers is more than procurement—it’s a strategic partnership. With its inhaler form and 100 μg per inhalation, 200 μg per inhalation 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 Salbuterol Inhalers