As a US pharma buyer, you're facing 25% API price hikes and supply delays for netarsudil in glaucoma treatments. Global Technology Co., Ltd delivers pharma-grade netarsudil API direct from GMP factories – cut costs by 30-40%, FDA-DMF compliant, no MOQ barriers for trials.
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You, as a procurement manager for US pharma firms, know the drill: netarsudil demand is surging with glaucoma cases hitting 80 million globally by 2026 (per WHO projections). But unreliable supply kills your ROI.
Ready to fix this? Scroll to our netarsudil solution – or get a quote now.
Netarsudil (CAS: 1259389-51-8, also known as netarsudil mesylate) is a breakthrough rho-associated kinase (ROCK) inhibitor API revolutionizing glaucoma and ocular hypertension management. Developed by Aerie Pharmaceuticals and launched as Rhopressa® in 2017, it targets elevated intraocular pressure (IOP) – the leading cause of irreversible blindness affecting 3 million Americans today, projected to rise 25% by 2026 (Glaucoma Research Foundation data).
Unlike traditional prostaglandins (e.g., latanoprost), netarsudil offers a multi-mechanism approach: it inhibits trabecular meshwork contraction, enhances aqueous humor outflow via the conventional pathway, and reduces episcleral venous pressure. Clinical trials (Rocket 1-4 studies) showed 8-9 mmHg IOP reduction at 0.02% ophthalmic solution dose – superior to monotherapy alternatives with fewer side effects like hyperemia (only 15-20% incidence vs. 40% for prostaglandins).
By 2026, the global glaucoma therapeutics market hits $12.5 billion (Grand View Research), with netarsudil generics capturing 15% share due to patent expiry in key markets. As an API supplier, netarsudil dimesylate (mesylate salt form for stability) is essential for formulating preservative-free eye drops, combination therapies (e.g., with latanoprost as Rocklatan®), and research into neurodegenerative applications. Its molecular formula C28H27N5O3 • CH4O3S (MW: 577.63 g/mol) demands >99% HPLC purity to meet USP/EP pharmacopeia.
Pharmacokinetics: Once-daily dosing with peak plasma levels <0.5 ng/mL ensures systemic safety. Stability data: 24 months shelf-life at 2-8°C, light-sensitive (amber packaging required). Regulatory: FDA-approved (NDA 208292), EMA orphan status. Market drivers include aging populations (65+ segment up 30% in USA) and telemedicine diagnostics boosting early interventions.
Production challenges overcome: Synthesis involves 10-step process from 4-bromo-1H-indazole, with chiral resolution yielding (S)-enantiomer. Impurity profiling critical – our process limits AR-13324 impurities to <0.1%. Real-world efficacy: Mercury 3 study (2023) confirmed 25% better adherence vs. timolol.
Expand your pipeline: Netarsudil APIs suit CRO/CMO for Phase III trials, veterinary ophthalmology, and combo drugs. Cost analysis: Bulk pricing $1,500-2,500/kg (vs. $4,000+ retail) yields 35% margins on finished drops.
| Parameter | Specification |
|---|---|
| CAS No. | 1259389-51-8 (Free base); 860990-09-0 (Mesylate) |
| Purity (HPLC) | ≥99.5% |
| Molecular Weight | 454.55 g/mol |
| Appearance | White to off-white powder |
| Loss on Drying | ≤0.5% |
| Heavy Metals | ≤10 ppm |
| Chiral Purity | ≥99% ee (S-isomer) |
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US client XYZ Pharma: Sourced 50kg netarsudil API, launched generic drops 3 months early, saving $250K on expedited imports.
Primary: Glaucoma/ocular hypertension eye drops. Secondary: Research combos. Compliant for US compounding per FDA 503B.

Contact us for quote. MOQ 1g-100kg. Pay via T/T, LC. Ships DDP to USA ports.
$1,800/kg (100kg+). 30% deposit, balance post-CoA. Escrow available.
Air: 7 days ($0.8/g). Sea: 25 days (tons). Temp-controlled, IATA compliant.
12-month warranty, free re-ship if OOS. Tech support 24/7.
Yes, ODM for formulations. NDA signed for IP.
"Best netarsudil supplier! Quality beat our previous India source. Fast ship to CA." – Mike R., Supply Chain Mgr. ★★★★★
"99.6% purity confirmed. Cut costs 32%. Highly recommend for US generics." – Lisa T., Tech Dir. ★★★★★
"Prompt service, free sample worked perfectly. Scaling to tons now." – Raj P., Ops Lead. ★★★★★
"DMF docs seamless for FDA. Delivery under 10 days!" – Emma K. ★★★★★
Free 10g sample for qualified buyers. 100% money-back if purity <99%. No risk – ships this week!
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Vice President, API Sourcing at Global Technology Co., Ltd. 25+ years in pharmaceutical intermediates, ex-GMP auditor for FDA/EMA, authored 15 papers on ROCK inhibitors. Personally oversees netarsudil production.
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