Showing all 31 results
Diphenylhydantoin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Dissolution-Optimized Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the highly reactive sodium salt.
Active Ingredient Strength Primary Clinical Function Diphenylhydantoin (Phenytoin) Sodium USP/Ph.Eur. 100 mg The Global Epilepsy Standard: The definitive therapeutic unit utilized globally for the chronic, daily maintenance and suppression of tonic-clonic and psychomotor seizures. Excipients Microcrystalline Cellulose / Lactose Monohydrate / Sodium Starch Glycolate / Povidone / Magnesium Stearate Diluent / Binder / Superdisintegrant / Glidant / Lubricant (Engineered specifically utilizing Strict Particle-Size Distribution (PSD) Control. Because the drug is highly insoluble, the API is micro-milled to an exact, mathematically defined micron size to guarantee a highly predictable, extended dissolution profile in the gut, preventing toxic “dose dumping”) *Pack Sizes: Bottles of 100 or 10×10 Blisters (Optimized specifically for strict chronic neurology dispensing regimens and therapeutic drug monitoring protocols).
Elevat
FreeThe term Elevat most commonly refers to Elevat 20 Capsule, a prescription antidepressant. However, depending on the specific product name (such as “Elevat D”), it may contain entirely different active ingredients like vitamins
Ergotamine & Caffeine ,Paracetamol & Prochlorperazine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Quad-API Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the sensitive ergot alkaloid and phenothiazine components.
Active Ingredient Strength Primary Clinical Function Ergotamine Tartrate USP/Ph.Eur. 1 mg The Vascular Terminator (Micro-Dose): The foundational ergot alkaloid required to aggressively constrict pulsing cranial arteries. Caffeine Anhydrous USP/Ph.Eur. 100 mg The Absorption Catalyst: Enhances Ergotamine bioavailability and accelerates onset of action. Paracetamol (Acetaminophen) USP/Ph.Eur. 250 mg The Central Analgesic (Macro-Dose): Provides immediate, broad-spectrum relief from accompanying head and neck pain. Prochlorperazine Maleate USP/Ph.Eur. 2.5 mg The Antiemetic Anchor (Ultra-Micro-Dose): Lethally blocks the CTZ to prevent vomiting and ensure full gastrointestinal absorption of the FDC. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Povidone K-30 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Lubricant (Engineered utilizing extreme multi-stage geometric dilution to flawlessly blend a microscopic 1mg and 2.5mg payload into a massive 250mg/100mg base, guaranteeing absolute content uniformity and zero toxic ‘hot spots’) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, heavily limited acute neurology dispensing to prevent ergot toxicity).
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).
Gabapentin & Amitriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 300 mg / 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Amitriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Amitriptyline is flawlessly distributed throughout the massive Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin & Nortriptyline Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose FDC Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of both active pharmaceutical ingredients.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 400 mg The Neuromodulator (Macro-Dose): The foundational calcium-channel inhibitor required to stabilize hyperactive nerve terminals. Nortriptyline (as Hydrochloride) USP/Ph.Eur. 10 mg The Synaptic Enhancer (Micro-Dose): The highly potent TCA required to amplify descending pain inhibition and restore sleep patterns. Excipients Microcrystalline Cellulose / Crospovidone / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / High-Shear Binder / Glidant / Film-Coating (Engineered specifically utilizing advanced multi-stage geometric dilution to ensure the lethal 10mg micro-dose of Nortriptyline is flawlessly distributed throughout the massive 400mg Gabapentin matrix, preventing toxic “hot spots”) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic neurology dispensing regimens).
Gabapentin Capsules
FreeGabapentin capsules (commonly 100 mg, 300 mg, and 400 mg) contain the active pharmaceutical ingredient gabapentin USP, along with a variety of inactive excipients that aid in the drug’s delivery and stability.
Gabapentine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, High-Density Macrodose Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the heavily compressed active pharmaceutical ingredient.
Active Ingredient Strength Primary Clinical Function Gabapentin USP/Ph.Eur. 600 mg Global Neuropathy Standard: The definitive high-dose unit utilized for the aggressive, long-term maintenance of severe diabetic peripheral neuropathy and postherpetic neuralgia. Gabapentin USP/Ph.Eur. 800 mg Max-Dose Seizure & Refractory Pain Standard: Massive therapeutic payload utilized for high-dose titration (up to 3600 mg/day) in refractory partial-onset seizures and extreme nerve pain. Excipients Copovidone / Crospovidone / Microcrystalline Cellulose / Magnesium Stearate / Premium Polymeric Film High-Shear Binder / Superdisintegrant / Diluent / Slipper-Coating (Engineered specifically utilizing advanced wet-granulation to compress the massive, fluffy 800mg API into a dense, smooth, swallowable tablet, preventing the pill from becoming a dangerous choking hazard for elderly patients) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for chronic, high-volume daily dispensing regimens).
L-Methylfolate Calcium ,Pyridoxal-5-Phosphate & Mecobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three delicate coenzymes.
Active Ingredient Strength Primary Clinical Function L-Methylfolate Calcium USP/Ph.Eur. 1 mg Active Vitamin B9: Direct methyl-donor for homocysteine remethylation and massive neurotransmitter synthesis. Pyridoxal-5-Phosphate (P5P) USP/Ph.Eur. 0.5 mg Active Vitamin B6: Immediate catalyst for transsulfuration; drastically reduces the risk of paradoxical sensory neuropathy seen with cheap Pyridoxine. Mecobalamin (Methylcobalamin) USP/Ph.Eur. 1500 mcg Active Vitamin B12: Direct peripheral nerve repair, myelin synthesis, and essential co-factor for homocysteine neutralization. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the active B12 and folate components) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology and diabetic dispensing regimens).
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).
Maxgalin
FreeMaxgalin is a brand of medication manufactured by Sun Pharmaceutical Industries Ltd., primarily used to treat neuropathic (nerve) pain, fibromyalgia, and certain types of seizures.
Methylcobalamin, Folic Acid & Pyridoxine TabletsÂ
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the three distinct vitamin coenzymes.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Active B12) Ph.Eur./USP 1500 mcg Myelin Regenerator: Direct peripheral nerve repair and essential co-factor for homocysteine remethylation. Folic Acid (Vitamin B9) Ph.Eur./USP 5 mg Endothelial Shield: Mega-dose methyl-donor driving DNA synthesis, red blood cell formation, and toxic homocysteine clearance. Pyridoxine Hydrochloride (Vitamin B6) Ph.Eur./USP 3 mg Neurotransmitter Catalyst: Vital co-enzyme for the transsulfuration of homocysteine and the synthesis of GABA/Serotonin. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / Heavy UV-Blocking Coating (Engineered specifically to form an impenetrable light barrier, completely preventing the photolabile degradation of the B12 component) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
Methylcobalamine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable Film-Coated Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the delicate coenzyme.
Active Ingredient Strength Primary Clinical Function Methylcobalamin (Mecobalamin) Ph.Eur./USP 500 mcg Maintenance / Hematology Standard: Base therapeutic unit for the treatment of Megaloblastic/Pernicious anemia and general nutritional B12 deficiency. Methylcobalamin (Mecobalamin) Ph.Eur./USP 1500 mcg Global Neurology Standard: Mega-dose adult therapy for the aggressive regeneration of peripheral nerves in Diabetic Neuropathy, Sciatica, and Trigeminal Neuralgia. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Magnesium Stearate / Titanium Dioxide / Premium Opaque Opadry Film Diluent / Superdisintegrant / Lubricant / UV-Blocking Coating (Engineered specifically to form a heavy, opaque shield that completely locks out ultraviolet light, preventing the photolabile degradation of the active coenzyme) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict, 3-to-6 month chronic neurology dispensing regimens).
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 Capsules
FreePregabalin and methylcobalamin capsules are a common combination therapy used to manage neuropathic pain (nerve pain). They are most frequently available in strengths of 75 mg / 750 mcg or 75 mg / 1500 mcg.
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).
Procyclidine 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 hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Procyclidine HCl BP/Ph.Eur. 5 mg Global Clinical Standard: Base therapeutic unit for the rapid reversal of EPS and parkinsonian rigidity. Excipients Lactose Monohydrate / Sodium Starch Glycolate / Povidone / Magnesium Stearate Diluent / Superdisintegrant / Binder / Lubricant (Engineered for rapid gastric dissolution and ultra-fast crossing of the blood-brain barrier) *Pack Sizes: 10×10 Blisters or Bottles of 100 (Optimized specifically for high-volume daily dispensing in acute psychiatric and neurology wards).
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.
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) Zonisamide Capsules
FreeZonisamide capsules are antiepileptic medications used as adjunctive therapy for adults and adolescents with partial-onset seizures. They are chemically classified as sulfonamides.
