Azithromycin Intravenous bulk supplier for pharma manufacturers

Azithromycin Intravenous Suppliers & Bulk Manufacturers

Available Forms: Intravenous (IV)

Available Strengths: 500 mg/250 mL, 1000 mg/250 mL

Reference Brands: Zithromax, Z-Pak(US); Zidimax(EU)

Category: Medical Aid

Azithromycin Intravenous is available in Intravenous (IV) and strengths such as 500 mg/250 mL, 1000 mg/250 mL. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Azithromycin Intravenous is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Azithromycin Intravenous can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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Product Description: Azithromycin IV is approved in the EU and US for severe bacterial infections, including respiratory and skin infections. In the EU, brands like Zithromax are regulated by EMA, supported by dossiers demonstrating safety, efficacy, and manufacturing standards. In the US, FDA approval relies on extensive clinical data; generic options are available. Both regions require detailed dossiers, clinical trial results, manufacturing quality, and pharmacovigilance plans for approval and safety monitoring. Due to its broad-spectrum activity and excellent tissue penetration, strict prescribing and monitoring guidelines are enforced. For regulatory support, dossier preparation, and compliance services, visit PharmaTradz. We ensure seamless market access adhering to European and US standards for safe, effective therapy.

Frequently Asked Questions

Yes, Azithromycin Intravenous is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Azithromycin Intravenous is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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