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Ranibizumab bulk supplier for pharma manufacturers

Ranibizumab Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 10 mg/mL

Reference Brands: Lucentis (USA/EU)

Category: Opthalmology

Ranibizumab is available in Injection and strengths such as 10 mg/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, Ranibizumab 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)

Ranibizumab 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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📘 Sourcing Guide

Product Description:

Ranibizumab is a vascular endothelial growth factor (VEGF-A) inhibitor used to manage and treat a variety of retinal disorders caused by abnormal blood vessel growth. Its approved indications include neovascular age-related macular degeneration (AMD), macular edema following retinal vein occlusion (RVO), diabetic macular edema (DME), myopic choroidal neovascularization, and diabetic retinopathy.

Ranibizumab works by binding to VEGF-A, preventing it from stimulating the formation of new blood vessels in the retina. This action reduces fluid leakage, limits retinal damage, and helps slow the progression of vision loss. Administered as a sterile intravitreal injection, ranibizumab requires careful monitoring to ensure safety and efficacy, including assessment of ocular and systemic adverse events.

Its well-established mechanism, targeted therapeutic effect, and wide range of ocular indications make ranibizumab a cornerstone in the management of retinal vascular diseases. Proper understanding of its pharmacodynamics, pharmacokinetics, dosing, adverse effect profile, and contraindications enables healthcare professionals to optimize patient outcomes in ophthalmology.

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Frequently Asked Questions

Ranibizumab is used to treat retinal vascular disorders, including wet age‑related macular degeneration (AMD), diabetic macular edema (DME), macular edema following retinal vein occlusion (RVO), and diabetic retinopathy by inhibiting VEGF and reducing abnormal blood vessel growth.

The active ingredient is ranibizumab, a recombinant humanized monoclonal antibody fragment targeting VEGF‑A. It is formulated as a sterile solution for intravitreal injection.

The most recognized trade name is Lucentis®.

Ranibizumab is produced by licensed biopharmaceutical manufacturers that hold marketing authorizations for Lucentis® and biosimilar ranibizumab products in various regions.

The generic name is Ranibizumab.

Brand examples include Lucentis® and related biosimilar products.

Ranibizumab is manufactured in GMP‑certified biopharmaceutical facilities globally, ensuring quality and sterility for intravitreal use.

Yes, Ranibizumab 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, Ranibizumab 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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