Modalert 200mg: Modalert Australia Product Information
Price range: A$99.00 through A$674.00
Modalert 200mg is a wakefulness-promoting medicine containing Modafinil 200mg, manufactured by Sun Pharmaceutical Industries Ltd. For people researching Modalert Australia, this page sets out the medicine’s recognised uses, how response can vary between individuals, and the safety considerations relevant to an informed discussion with a qualified healthcare professional.
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Product Highlights
| Specification | Details |
| Active Ingredient | Modafinil 200mg |
| Strength | 200mg tablet |
| Manufacturer | Sun Pharmaceutical Industries Ltd. |
| Dosage Form | Oral tablet |
| Medicine Type | Wakefulness-promoting medicine |
Description
What Is Modalert 200mg?
Modalert Australia is a branded modafinil tablet. Sun Pharmaceutical Industries’ official India product catalogue lists MODALERT 200 MG TABLET with modafinil, a labelled strength of 200mg and tablet dosage form.
This product catalogue supports the association between the Modalert brand, modafinil, the 200mg strength and Sun Pharmaceutical Industries’ product portfolio. It does not by itself establish a particular manufacturing site, Australian ARTG registration or Australian-approved indications for Modalert.
The pharmacological effects associated with Modalert relate to modafinil. Although its precise mechanism remains incompletely understood, modafinil influences several neural and neurotransmitter systems involved in wakefulness.
Individual response to modafinil treatment varies. The underlying cause of excessive daytime sleepiness, medical history, other medicines and individual clinical circumstances should therefore be assessed by an appropriately qualified healthcare professional before treatment.
How Long Does Modalert Take to Work?
There is no single verified Modalert-specific onset time that applies to every person. It is useful to distinguish several different concepts when discussing timing:
- Perceived onset refers to when an individual first notices a change in alertness.
- Pharmacokinetic timing describes how the active ingredient is absorbed and reaches concentrations in the body.
- Duration of effect refers to how long wakefulness-related effects are experienced.
- Clinical response describes whether treatment adequately controls excessive sleepiness over ongoing medical review.
General modafinil pharmacokinetic information should not be treated as proof of an exact onset, peak time or duration for Modalert 200mg. Factors such as individual physiology, health conditions and other medicines may be relevant to treatment response, but they do not establish a predictable subjective onset time for every patient.
For broader educational context about onset, pharmacokinetic timing and subjective effects, see how long Modvigil 200mg takes to work. Modvigil is a separate branded product, so that information should not be interpreted as Modalert-specific onset evidence or as evidence that the two products are bioequivalent.
Recognised Medical Uses
Recognised Modafinil Treatment Contexts
Modafinil is used in recognised medical settings involving excessive daytime sleepiness. These include:
- Narcolepsy
- Excessive daytime sleepiness associated with obstructive sleep apnoea as part of broader management
- Shift work sleep disorder in appropriately selected patients
For obstructive sleep apnoea, wakefulness-promoting treatment addresses excessive sleepiness rather than the underlying airway obstruction. Appropriate management of the underlying condition, including CPAP where prescribed or recommended, remains important.
These medical contexts relate to modafinil and relevant clinical or registered-product evidence. They do not establish that Modalert 200mg itself has Australian-approved indications or ARTG registration.
For broader ingredient-level educational information, see Modvigil 200mg uses, benefits and side effects.
Potential Treatment Outcomes
In recognised clinical settings, modafinil may help suitable patients improve wakefulness and reduce excessive daytime sleepiness during appropriate waking hours.
Individual responses vary, and successful treatment depends on the underlying condition and broader management plan. Wakefulness-promoting treatment does not replace adequate sleep, healthy sleep practices or treatment directed at the underlying sleep disorder.
Ongoing medical review helps determine whether treatment is effective, well tolerated and still appropriate.
How to Use Modalert
Modalert 200mg should be used according to the instructions provided by the prescribing healthcare professional and valid product-specific labelling supplied with the medicine.
The verified Sun Pharmaceutical Industries catalogue establishes the Modalert product name, modafinil, 200mg strength and tablet dosage form, but it does not establish detailed administration instructions such as whether the tablet should be divided, crushed, taken with food or taken at a particular time.
The appropriate treatment regimen should be determined individually. Clinical considerations may include the diagnosed condition, treatment response, age, medical history, liver function and other medicines being used, but these factors should not be interpreted as Modalert-specific dosing instructions.
For readers reviewing another listed strength in the same branded product family, see Modalert 100mg. A 100mg and 200mg product listing does not establish dose equivalence, interchangeability or identical formulation, and patients should not substitute strengths without professional advice.
Possible Side Effects
Common Side Effects
Modafinil can cause side effects. Reported effects include headache, nausea, dizziness, nervousness or anxiety, difficulty sleeping and gastrointestinal symptoms.
Not everyone experiences side effects, and their type and severity can vary.
For broader ingredient-level safety information, see Modvigil 200mg side effects.
Serious Side Effects
Serious reactions have been reported with modafinil, including severe skin reactions, serious hypersensitivity reactions, significant psychiatric symptoms and cardiovascular problems.
Seek prompt medical attention for serious or unexpected symptoms such as a severe or spreading rash, facial or throat swelling, difficulty breathing, chest pain, marked changes in mood or behaviour, hallucinations or suicidal thoughts.
These warnings reflect modafinil safety information and should not be interpreted as independent Modalert-specific pharmacovigilance data.
Warnings & Precautions
Before modafinil treatment begins, tell your healthcare professional about your complete medical history and all medicines and supplements you use.
Heart Conditions
People with high blood pressure, cardiovascular disease or other significant heart-related conditions should discuss these with their healthcare professional before modafinil treatment. Individual circumstances may require additional assessment or monitoring.
Liver Disease
Liver function can be relevant to modafinil treatment because the medicine is processed in the body partly through hepatic pathways. People with liver disease should discuss their condition with the prescribing healthcare professional.
This information should not be interpreted as a specific Modalert dose-adjustment instruction.
Kidney Disease
People with kidney disease should inform their healthcare professional before treatment so that their overall medical condition and medicine use can be assessed.
Mental Health
A history of depression, significant anxiety, bipolar disorder, psychosis, mania or other important psychiatric conditions should be discussed before modafinil treatment.
Pregnancy
Australian regulatory information for the registered modafinil product MODAVIGIL was updated in 2025 to include pregnancy in its contraindications and to strengthen information concerning fetal harm, congenital malformations and spontaneous abortion. The TGA provides updated pregnancy safety information for modafinil.
This information concerns MODAVIGIL and should not be represented as Modalert Product Information. However, anyone who is pregnant, planning pregnancy or becomes pregnant while receiving modafinil should seek medical advice promptly.
Breastfeeding
People who are breastfeeding or planning to breastfeed should discuss modafinil treatment with their healthcare professional. Pregnancy safety information should not automatically be assumed to provide identical breastfeeding guidance.
Driving and Operating Machinery
An underlying sleep disorder can itself impair alertness, and individual responses to modafinil treatment vary. Patients should understand how both their condition and treatment affect them before driving, operating machinery or undertaking other safety-sensitive activities.
Other Medicines
Provide your healthcare professional or pharmacist with a complete list of prescription medicines, over-the-counter medicines, vitamins, herbal products and supplements before starting or changing modafinil treatment.
Drug Interactions
Modafinil may affect the metabolism or effects of other medicines. Potentially relevant interactions include certain anticoagulants, anti-epileptic medicines, antidepressants, hormonal contraceptives and other medicines affected by liver-enzyme pathways.
The clinical significance of an interaction depends on the medicines involved and individual circumstances. Patients should not attempt to assess or manage potentially important interactions without professional advice.
Hormonal Contraception
Modafinil can interact with hormonal contraception and may reduce the effectiveness of some hormonal contraceptive methods.
People using hormonal contraception should obtain individual contraceptive advice from an appropriately qualified healthcare professional, including whether an alternative or additional method is needed and how long additional precautions may be required after modafinil treatment ends.
Storage Instructions
- Follow the storage instructions printed on the supplied product packaging or label.
- Keep the medicine in its supplied packaging where appropriate.
- Keep medicines out of sight and reach of children.
- Do not use the product after the expiry date shown on the packaging.
Exact storage conditions should be taken from valid Modalert-specific product information rather than inferred from general medicine-storage advice.
Why People Compare Modalert
People researching Modalert 200mg may compare it with other products presented or labelled as containing modafinil. Relevant considerations can include labelled strength, formulation, product documentation, regulatory status and advice from an appropriately qualified healthcare professional.
A shared claimed active ingredient or labelled strength does not establish identical formulation, manufacturing arrangements, bioequivalence, interchangeability, therapeutic equivalence or identical regulatory status.
For a direct educational comparison involving the same labelled strength, see Modvigil 200mg vs Modalert 200mg. That comparison should not be interpreted as evidence that the two branded products are interchangeable or bioequivalent.
Product Information for Australian Consumers
When researching Modalert 200mg, focus on product identification and the applicable medical and regulatory requirements rather than general ecommerce features.
Useful points to check include:
- The exact product name
- The listed active ingredient: modafinil
- The labelled strength: 200mg
- The dosage form
- Product-specific labelling and documentation
- Batch and expiry information where supplied
- Applicable prescription and regulatory requirements
Sun Pharmaceutical Industries’ official India catalogue lists MODALERT 200 MG TABLET with modafinil at a labelled strength of 200mg. This catalogue association should not be extended into unsupported claims about an exact manufacturing site or Australian regulatory approval.
Packaging and labelling can assist with product identification, but visual consistency alone does not prove authenticity, ingredient composition, pharmaceutical quality or regulatory approval.
Frequently Asked Questions
What is Modalert 200mg?
Modalert 200mg is listed in Sun Pharmaceutical Industries’ official India catalogue as a tablet product with modafinil at a labelled strength of 200mg.
This listing does not establish Australian ARTG registration or Australian-approved indications for Modalert.
Who manufactures Modalert?
Sun Pharmaceutical Industries’ official India product catalogue lists Modalert 200mg within its product portfolio. The catalogue establishes this product association but does not by itself establish the exact manufacturing site or justify a stronger manufacturer claim.
What is Modalert used for?
Modafinil is used in recognised medical contexts involving excessive daytime sleepiness, including narcolepsy and selected cases of shift work sleep disorder and obstructive sleep apnoea.
These ingredient-level uses do not establish Australian-approved indications for Modalert 200mg.
How long does Modalert take to work?
There is no single verified Modalert-specific onset time that applies to everyone. Perceived onset, pharmacokinetic timing, duration of effects and assessment of longer-term clinical response are different concepts.
Treatment-specific expectations should be discussed with a healthcare professional.
What are the most common side effects?
Modafinil can cause effects such as headache, nausea, dizziness, nervousness or anxiety, difficulty sleeping and gastrointestinal symptoms. Individual experiences vary.
Is Modalert the same as generic modafinil?
No. Modalert is a branded finished product, while modafinil is the active pharmaceutical ingredient listed for the product.
Other branded or generic products may also be presented as containing modafinil, but a shared ingredient does not establish identical formulation, bioequivalence, interchangeability, therapeutic equivalence or identical regulatory status.
Is Modalert suitable for everyone?
No medicine containing modafinil is suitable for every person. Suitability depends on the underlying condition, medical history, other medicines and an individual clinical assessment by an appropriately qualified healthcare professional.
Medical Disclaimer
The information on this page is provided for general educational purposes only and does not replace personalised medical advice, diagnosis or treatment. It should not be used to self-diagnose, self-select a medicine or choose a tablet strength or treatment regimen.
Modafinil is a Schedule 4 Prescription Only Medicine in Australia. Decisions about whether modafinil treatment is appropriate, which product or strength should be used and how treatment should be monitored require assessment by an appropriately qualified healthcare professional.
Australian clinical, prescribing and regulatory information concerning modafinil or Australian-registered modafinil products does not establish that Modalert 200mg is ARTG registered or has Australian-approved indications.
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