Neurological & CNS

ArmodafinilThird Party Manufacturing in India

Looking to get Armodafinil manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
112111-43-0
Drug Class
Atypical dopamine reuptake inhibitor (wakefulness-promoting agent)
Molecular Formula
C₁₅H₁₅NO₂S
Molecular Weight
273.35 g/mol
Grade Standards
IP, USP
Therapeutic Category
Neurological & CNS
MOQ
Contact us for MOQ — varies by strength and dosage form
Dosage Forms
Tablet

Mechanism of Action

Armodafinil works by promoting wakefulness through the selective regulation of neurotransmitters in the brain. As the active R-enantiomer of modafinil, it acts primarily as an atypical dopamine reuptake inhibitor. By binding to the dopamine transporter protein, it blocks the reabsorption of dopamine into the nerves. This action increases the concentration of dopamine in the synaptic cleft, particularly in the prefrontal cortex, enhancing alertness and cognitive drive.

Unlike amphetamines and other traditional central nervous system stimulants, armodafinil does not cause direct release of dopamine or norepinephrine. It shows a highly selective profile, interacting with the orexin and histamine systems in the hypothalamus to promote wakefulness. This unique pharmacological behavior reduces the risk of rebound hypersomnia, cardiovascular side effects, and addictive potential. It is highly effective and well-tolerated for patients needing sustained wakefulness throughout the day without the jittery sensations typical of older psychostimulants.

Therapeutic Uses & Indications

Therapeutic Uses

Armodafinil is prescribed for the treatment of:

  • Narcolepsy: To improve wakefulness in adults experiencing excessive daytime sleepiness associated with this chronic neurological disorder.
  • Obstructive Sleep Apnea (OSA): To treat residual sleepiness in patients undergoing primary treatment such as continuous positive airway pressure (CPAP).
  • Shift Work Disorder (SWD): To alleviate excessive sleepiness in individuals whose work schedules disrupt their circadian rhythms.

Why Manufacturers Choose Armodafinil

Armodafinil is highly valued in the contract manufacturing sector due to its superior pharmacokinetic profile compared to racemic modafinil. It exhibits a longer half-life, meaning it provides more stable and sustained wakefulness with once-daily dosing. For pharmaceutical distributors, this translates into a premium product offering with high patient compliance.

As a prominent target for third party manufacturing in India, armodafinil tablets represent a growing niche within the neurological and wakefulness-promoting drug markets. The global demand for eugeroics is rising steadily, making this molecule a lucrative addition for export-oriented portfolios and local franchise catalogs alike. Celesta Healthcare offers WHO-GMP compliant manufacturing facilities to produce high-quality armodafinil tablets in multiple strengths, ensuring strict quality control and timely delivery.

Dosage Forms We Manufacture

Tablet
50mg · 100mg · 150mg · 200mg · 250mg

Frequently Asked Questions

What is the minimum order quantity for Armodafinil?
Minimum order quantity for Armodafinil is Contact us for MOQ — varies by strength and dosage form. Please contact us for bulk pricing and custom quantities.
What dosage forms of Armodafinil can you manufacture?
We manufacture Armodafinil as: Tablet (50mg, 100mg, 150mg, 200mg, 250mg).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Armodafinil for export?
Yes. We provide export-ready Armodafinil formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Armodafinil?
We manufacture Armodafinil to IP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Armodafinil made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • Low MOQ, export ready
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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Blister pack (Alu-Alu), Strip pack, HDPE bottle. Customized packaging formats available.

Start Manufacturing Armodafinil Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Armodafinil across all dosage forms. PCD franchise and export orders welcome.

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