Showing all 19 results
Amantadine Hydrochloride Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Immediate-Release Tablet, packed in moisture-resistant Alu-Alu or Alu-PVC blister strips.
Active Ingredient Strength Primary Clinical Function Amantadine Hydrochloride USP/BP 100 mg The Standard Therapeutic Anchor: The globally validated dose for both Parkinsonian motor control and antiviral prophylaxis. Excipients Proprietary Matrix Rapid-Release System: Engineered to ensure a consistent $T_{max}$ (peak concentration) of approx. 2 to 4 hours for reliable daily protection. Flunarazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Microdose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the dihydrochloride salt.
Active Ingredient Strength Primary Clinical Function Flunarizine (as Dihydrochloride) USP/Ph.Eur. 5 mg The Pediatric & Geriatric Standard: The definitive low-dose unit required for migraine prophylaxis in children or for treating vertigo in elderly patients who are highly sensitive to drug accumulation. Flunarizine (as Dihydrochloride) USP/Ph.Eur. 10 mg The Global Adult Migraine Standard: High-efficacy adult maintenance dose utilized for maximum suppression of chronic, refractory migraine attacks. Excipients Lactose Monohydrate / Microcrystalline Cellulose / Crospovidone / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered utilizing elite low-dose geometric dilution to guarantee that the 5mg or 10mg micro-dose is flawlessly distributed, preventing accidental drug-accumulation spikes) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, heavily monitored 3-to-6 month neurology dispensing regimens).
Ginkgo Biloba Extract ,Piracetam & Vinpocetine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the combined phyto-synthetic payloads.
Active Ingredient Strength Primary Clinical Function Piracetam USP/Ph.Eur. 400 mg / 800 mg The Nootropic Anchor: Massive synthetic payload required to force neuroplasticity, enhance membrane fluidity, and restore memory function in damaged neural networks. Ginkgo Biloba Extract (Standardized) 60 mg The Microcirculatory Botanical: Standardized extract to prevent capillary clotting and shield the brain from oxidative stress. Vinpocetine USP/Ph.Eur. 5 mg The Cerebral Oxygenator (Micro-Dose): Targeted vasodilation of cerebral arteries to immediately restore oxygen delivery to ischemic tissues. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Polyvinylpyrrolidone (PVP) / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Binder / Slipper-Coating (Engineered specifically to compress the incredibly bulky Piracetam alongside the sticky herbal extract into a single, dense, swallowable pill, heavily coated to lock out tropical humidity) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, chronic 3-to-6 month neurology dispensing regimens).
Ginkgo Biloba Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Pharmaceutical-Grade Botanical Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly hygroscopic herbal extract.
Active Ingredient Strength Primary Clinical Function Standardized Ginkgo Biloba Extract (Leaves) 40 mg The Tinnitus & Vertigo Standard: Base therapeutic unit frequently prescribed three times daily for the management of inner-ear microcirculatory disorders (tinnitus and dizziness). Standardized Ginkgo Biloba Extract (Leaves)
*Strictly Standardized to 24% Ginkgo Flavone Glycosides & 6% Terpene Lactones (EGb 761 Equivalent)80 mg / 120 mg The Cognitive & Vascular Standard: High-efficacy adult macro-doses utilized for the targeted treatment of vascular dementia, Alzheimer’s disease adjunct therapy, and intermittent claudication. Excipients Microcrystalline Cellulose / Crospovidone / Colloidal Anhydrous Silica / Magnesium Stearate / Premium Moisture-Barrier Film Diluent / Superdisintegrant / Glidant / Lubricant (Engineered utilizing strictly climate-controlled dry-granulation to prevent the intensely sticky botanical extract from agglomerating, heavily coated to lock out humidity and prevent the characteristic pungent botanical odor) *Pack Sizes: 10×10 Blisters or Bottles of 60 (Optimized specifically for chronic, lifelong neuro-vascular maintenance).
Lamotrigine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Rapid-Dispersible (DT) Tablet, packed exclusively in highly secure Alu-PVC or Alu-Alu blister strips, frequently customized into highly regulated Titration Starter Kits.
Active Ingredient Strength Primary Clinical Function Lamotrigine USP/Ph.Eur. 25 mg (Starter Kit) The SJS-Prevention Standard: Mandatory base unit for the strict, slow titration schedule required to prevent fatal cutaneous reactions. Often formulated as a Dispersible Tablet (DT) for pediatric epilepsy. Lamotrigine USP/Ph.Eur. 50 mg / 100 mg / 200 mg Global Maintenance Standard: High-efficacy adult maintenance doses for lifelong seizure control and bipolar stabilization. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Povidone / Sucralose & Flavoring (If DT) / Magnesium Stearate Diluent / Superdisintegrant / Binder / Sweetener (Engineered specifically to either swallow intact or disperse rapidly in a teaspoon of water for children or elderly psychiatric patients suffering from dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 100, or Dedicated 28-Day Titration Calendar Packs (Optimized specifically to eliminate caregiver dosing errors during the critical initiation phase).
Memantine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips, frequently customized into 4-week Titration Starter Packs.
Active Ingredient Strength Primary Clinical Function Memantine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized exclusively for the mandatory 4-week step-up protocol to build patient tolerance and prevent severe CNS adverse effects. Memantine (as Hydrochloride) USP/Ph.Eur. 10 mg Global Neurology Standard: High-efficacy adult maintenance dose, typically taken twice daily, for the sustained neuroprotection of the degenerating brain. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Croscarmellose Sodium / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Superdisintegrant / Slipper-Coating (Engineered specifically with a heavy, smooth film-coat to ensure immediate gastric transit and absolute ease of swallowing for elderly patients suffering from severe dysphagia) *Pack Sizes: 10×10 Blisters, Bottles of 60, or Customized 28-Day Titration Starter Kits (Optimized specifically for strict chronic geriatric dispensing regimens).
Neostigmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or high-density PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic bromide salt.
Active Ingredient Strength Primary Clinical Function Neostigmine Bromide Ph.Eur./USP 15 mg Global Clinical Standard: Base therapeutic oral unit for the continuous, meticulously spaced symptomatic management of Myasthenia Gravis. Excipients Lactose Monohydrate / Maize Starch / Povidone K30 / Talc / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered specifically for rapid, predictable gastric dissolution to ensure precise symptom control within 30 to 45 minutes of ingestion) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for strict, high-volume chronic neurology dispensing, as patients may require up to 10-15 tablets per day in divided doses).
Piracetam Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu or heavy-gauge PVC/PVDC blister strips to ensure the absolute chemical stability of the highly hygroscopic API.
Active Ingredient Strength Primary Clinical Function Piracetam Ph.Eur./USP 400 mg Initiation / Pediatric Standard: Base unit for pediatric dyslexia and mild vertigo management. Piracetam Ph.Eur./USP 800 mg Global Cognitive Standard: Standard adult maintenance dose for age-related cognitive decline and memory impairment. Piracetam Ph.Eur./USP 1200 mg Acute Neurology Standard: Massive-dose unit designed specifically for Cortical Myoclonus and intensive post-stroke rehabilitation protocols to minimize pill burden. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Macrogol (PEG) / Colloidal Silicon Dioxide / Magnesium Stearate High-Density Diluent / Superdisintegrant / Premium Film-Coating (Engineered specifically to compress the massive API load into a smooth, swallowable, moisture-resistant oblong tablet) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict, high-volume chronic neurology dispensing where patients may consume 2.4g to 4.8g daily).
Pramipexole Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly light-sensitive dihydrochloride monohydrate salt.
Active Ingredient Strength Primary Clinical Function Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 0.125 mg Micro-Dose Standard: Mandatory initiation unit to prevent orthostatic shock, and the gold-standard maintenance dose for RLS. Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 0.25 mg / 0.5 mg Titration Standard: Mid-level doses for the gradual, safe escalation of Parkinson’s therapy. Pramipexole (as Dihydrochloride Monohydrate) Ph.Eur./USP 1 mg Advanced PD Standard: High-dose maintenance therapy for severe, refractory Parkinson’s Disease. Excipients Mannitol / Maize Starch / Povidone K25 / Colloidal Silicon Dioxide / Magnesium Stearate Diluent / Binder / Glidant / Lubricant (Engineered for immediate gastric dissolution and rapid, highly predictable systemic absorption) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict, high-compliance chronic neurology dispensing and complex titration regimens).
Pregabalin & Methylcobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly light-sensitive B12 coenzyme and the SR polymer network.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 75 mg (Sustained-Release) 24-hour controlled suppression of neuropathic pain and hyperalgesia. Methylcobalamin (Mecobalamin) JP/USP 1500 mcg Global Clinical Standard: High-dose active B12 for the anatomical regeneration of the myelin sheath. Excipients Hypromellose (HPMC) / Microcrystalline Cellulose / Colloidal Silicon Dioxide / Titanium Dioxide / Magnesium Stearate Hydrophilic SR Polymer Matrix / Diluent / Glidant / UV-Blocking Film-Coating (Engineered to control the exact 24-hour diffusion rate while shielding the API from light degradation) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic diabetology and neurology dispensing regimens).
Pregabalin & Nortriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure absolute chemical stability and to mask the extremely bitter taste of the TCA component.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 50 mg / 75 mg Calcium channel neuromodulation for the direct suppression of hyperactive nerve firing. Nortriptyline Hydrochloride BP/USP 10 mg (Base Equivalent) Global Clinical Standard: SNRI/TCA action to amplify the brain’s natural descending pain-inhibiting pathways. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K30 / Magnesium Stearate / Titanium Dioxide Diluent / Superdisintegrant / Binder / Premium Film-Coating (Engineered specifically to ensure immediate, synchronized gastric dissolution while completely masking the bitter taste of Nortriptyline) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Pregabalin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Hard Capsule or Extended-Release Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the active amino acid derivative and prevent illicit tampering.
Active Ingredient Strength Primary Clinical Function Pregabalin INN/Ph.Eur. 75 mg Initiation Standard: Base titration unit to safely acclimatize the brain and minimize initial dizziness. Pregabalin INN/Ph.Eur. 150 mg / 300 mg Global Clinical Standard: Advanced maintenance doses for severe diabetic neuropathy, fibromyalgia, and refractory epilepsy. Excipients (Capsules) Pregelatinized Starch / Talc / Hard Gelatin Shell Diluent / Glidant / Capsule Matrix (Engineered for immediate gastric dissolution and rapid systemic onset within 1 hour) *Pack Sizes: 10×10 Alu-Alu Blisters or 14-Capsule Titration Packs (Optimized specifically for strict chronic pain dispensing regimens and controlled-substance tracking).
Pyridostigmine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-density HDPE bottles with desiccants to ensure the absolute chemical stability of the highly hygroscopic bromide salt.
Active Ingredient Strength Primary Clinical Function Pyridostigmine Bromide USP/Ph.Eur. 60 mg Global Clinical Standard: Base maintenance dose for continuous 24-hour neuromuscular control in MG patients. Excipients Silicone Dioxide / Microcrystalline Cellulose / Pregelatinized Starch / Magnesium Stearate Glidant / Diluent / Binder / Lubricant (Engineered for immediate gastric dissolution and precise, rapid systemic onset within 30-45 minutes) *Pack Sizes: Bottles of 100 or 10×10 Alu-Alu Blisters (Optimized specifically for strict, high-volume daily neurology regimens where patients may consume 6 to 10 tablets daily).
Rasagiline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Uncoated or Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly sensitive mesylate salt.
Active Ingredient Strength Primary Clinical Function Rasagiline Mesylate INN/Ph.Eur. 0.5 mg (Base Equivalent) Adjunct Standard: Initiating dose when used in combination with Levodopa. Rasagiline Mesylate INN/Ph.Eur. 1 mg (Base Equivalent) Global Clinical Standard: Maximum daily dose for monotherapy or advanced adjunct therapy. Excipients Mannitol / Maize Starch / Pregelatinized Starch / Colloidal Silicon Dioxide / Stearic Acid Diluent / Binder / Superdisintegrant / Glidant (Engineered for immediate gastric dissolution and rapid crossing of the blood-brain barrier) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict high-compliance 30-day chronic neurology dispensing regimens).
Ropinirole Extended-Release
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Polymeric Matrix Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips or heavy-gauge HDPE bottles to ensure the absolute stability of the modified-release polymers.
Active Ingredient Strength Primary Clinical Function Ropinirole HCl USP/Ph.Eur. 2 mg / 4 mg Base titration units for the slow, safe initiation of dopaminergic therapy. Ropinirole HCl USP/Ph.Eur. 8 mg Global Clinical Standard: Advanced maintenance dose for 24-hour continuous symptom control. (Higher total daily doses may be required). Excipients Hypromellose (HPMC) / Carmellose Sodium / Lactose Monohydrate / Magnesium Stearate Hydrophilic Polymer Matrix / Diluent / Lubricant (Engineered to form a viscous gel layer that controls the strict 24-hour drug diffusion rate) *Pack Sizes: 10×10 Alu-Alu Blisters or Bottles of 28/30 (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Sumatriptan & Naproxen Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer or Matrix Film-Coated Tablet, packed exclusively in highly secure, child-resistant Alu-Alu or high-density Alu-PVC blister strips to ensure the absolute kinetic stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Sumatriptan Succinate USP/Ph.Eur. 85 mg (Equivalent to Sumatriptan base) Rapid-onset 5-HT1 agonism for the immediate abortion of the migraine attack. Naproxen Sodium USP/Ph.Eur. 500 mg Long-acting COX inhibition for sustained neuro-inflammatory blockade and rebound prevention. Excipients Croscarmellose Sodium / Microcrystalline Cellulose / Povidone / Magnesium Stearate Superdisintegrant / Diluent / Binder (Engineered for immediate gastric dissolution and synchronized absorption) Sumatriptan Tablets
FreeA Sumatriptan tablet (often known by the brand name Imitrex) is a prescription medication used to treat acute migraine attacks. It belongs to the triptan class of drugs, which are selective serotonin (5-HT1B/1D) receptor agonists.
Tetrabenazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Scored Tablet, packed in highly secure, moisture-resistant Alu-PVC or opaque Alu-Alu blister strips, optimized for strict neurological dose titration and chronic dispensing.
Active Ingredient Strength Primary Clinical Use Tetrabenazine INN/Ph.Eur. 25 mg Standard Titration & Maintenance: Scored to allow for precise 12.5 mg micro-dosing during the critical initiation phase. Excipients Lactose / Maize Starch / Magnesium Stearate / Iron Oxide Yellow Diluent / Glidant / Colorant (Engineered for immediate gastric dispersion and precise tablet splitting) Topiramate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet, packed in highly secure, moisture-resistant Alu-Alu blister strips to guarantee absolute stability of the active pharmaceutical ingredient across diverse climate zones.
Active Ingredient Strength Primary Clinical Use Topiramate USP/Ph.Eur. 25 mg Titration & Migraine: Mandatory low-dose initiation to prevent cognitive side effects. Topiramate USP/Ph.Eur. 50 mg Standard Adult Maintenance Dose for chronic migraine prophylaxis. Topiramate USP/Ph.Eur. 100 mg / 200 mg High-dose therapy for refractory epilepsy and generalized tonic-clonic seizures. Excipients Lactose Monohydrate / Pregelatinized Starch / Sodium Starch Glycolate Diluent / Superdisintegrant (Engineered for immediate, uniform gastric dispersion)
