Ibuprofen
I have found results from1000+products and400+suppliers aboutIbuprofen
Apis & Intermediates: Paracetamol and Ibuprofen Pain Relief
Pharmaceutical Grade Ibuprofen Active Pharmaceutical Ingredient
Factory Wholesale Pharmaceutical Raw Material Ibuprofen Powder CAS 15687-27-1
Nsaids GMP Certificate High Quality OEM Ibuprofen Injection 800mg/8ml
Premium 400mg Ibuprofen Tablets for Fast Pain Relief - 10X10 Pack
Ibuprofen Powder CAS 15687-27-1 Ibuprofen Purity Ibuprofen Material Ibuprofen
Factory Supply Ibuprofen Bulk Export Flexible MOQ for Trial & Bulk Orders
Export Grade Ibuprofen Non-Hazardous Pharmaceutical Raw Material Custom Neutral Packaging
High Safety Ibuprofen Sustained Release Capsules for Headache Relief
Long Lasting Ibuprofen Sustained Release Capsules for Neuralgia Relief
Low Side Effect Ibuprofen Sustained Release Capsules for Myalgia Relief
Lowest Price Pharmaceutical Material Supply Ibuprofen CAS 15687-27-1
Wholesale Medicine GMP Pharmaceutical Drug 400mg Ibuprofen Tablets
Chemical Intermediate Ibuprofen Powder CAS 15687-27-1 Ibuprofen Purity Material
High Safety Ibuprofen Sustained Release Capsules for Pain Relief
Low Gi Irritation Ibuprofen Sustained Release Capsules for Headache Relief
Sourcing guidance for Ibuprofen
What are the critical quality standards and certifications for sourcing Ibuprofen?
When sourcing Ibuprofen, you must ensure the supplier complies with GMP (Good Manufacturing Practice) standards. The product should ideally have a CEP (Certificate of Suitability to the Monographs of the European Pharmacopoeia) or a US DMF (Drug Master File) number. For the material itself, it must meet the latest pharmacopoeia standards such as USP (United States Pharmacopeia), BP (British Pharmacopoeia), or EP (European Pharmacopoeia) to ensure purity, limit of impurities (like 4-isobutylacetophenone), and correct melting point.
How should buyers evaluate the technical specifications of Ibuprofen powder?
Buyers should focus on Particle Size Distribution (PSD), as it directly affects the flowability and compressibility for tablet manufacturing. Common grades include 25 mesh, 40 mesh, and 80 mesh. Additionally, verify the Assay content (typically 98.5% to 101.0% on an anhydrous basis) and the Heavy Metals limit (≤10ppm). Requesting a Certificate of Analysis (COA) from the specific batch is mandatory before shipment.
What are the compliance requirements for importing Ibuprofen into different regions?
Importing Ibuprofen requires strict adherence to local health authorities. In the US, the facility must be FDA registered. In the EU, an Import Authorization and a Written Confirmation (WC) from the exporting country's health authority are required. For many developing markets, a CPP (Certificate of Pharmaceutical Product) issued by the WHO format is essential for product registration.
Cross-Border Procurement Risks and Strategic Advice for Ibuprofen
What are the primary risks in cross-border chemical and pharmaceutical sourcing?
The biggest risks include regulatory non-compliance and quality degradation during transit. Pharmaceutical ingredients are sensitive to environmental factors; therefore, you must ensure the supplier uses tamper-evident packaging and provides stability data. Always use secure payment terms like Letter of Credit (L/C) or platforms like Made-in-China.com that offer trade security services to mitigate financial risks.
How can I ensure smooth customs clearance for Ibuprofen shipments?
Ensure all documentation is perfectly aligned. This includes the HS Code (typically 29163930 for Ibuprofen), Commercial Invoice, Packing List, and MSDS (Material Safety Data Sheet). Because Ibuprofen is a regulated substance, missing a Health Certificate or an Import License can lead to immediate seizure by customs. Always verify the specific import tariffs and anti-dumping duties applicable to your country.
What strategies should be used when negotiating with pharmaceutical suppliers?
Focus on long-term supply stability rather than just the lowest price. Ask about the supplier's annual production capacity to ensure they can handle scale-ups. Negotiate for re-testing periods (allowing you 15-30 days to conduct your own lab analysis upon receipt) before the final payment is released. For bulk orders, aim for tiered pricing where costs drop significantly at the 1-ton, 5-ton, and 10-ton thresholds.





























