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Cefoperazone & Tazobactam Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Dry Powder for Injection in glass vials. The standard ratio is 8:1.
Strength Variant Cefoperazone Content Tazobactam Content Ratio 1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – *Pack Sizes: Tray of 1 Vial, 10 Vials, or Box of 1/10 Vials with Water for Injection (WFI).
1.125 g Vial 1000 mg (1 g) 125 mg (Sodium) 8:1 (Standard) Excipients None (Sterile Blend) – – DEFERASIROX TABLETS
FreeProduct Composition & Strength
We supply this product across two distinct, Precision-Blended Engineering Platforms, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute physical and chemical stability of the active pharmaceutical ingredient.
Active Ingredient Strength & Form Primary Clinical Function Deferasirox USP/Ph.Eur. 125 mg / 250 mg / 500 mg (Dispersible) The Pediatric Suspension Standard: Engineered with micro-crystalline disintegrants to rapidly dissolve in water or apple juice for precise, weight-based pediatric dosing. Deferasirox USP/Ph.Eur. 90 mg / 360 mg (Film-Coated) The High-Compliance Macrodose: The highly densified, lactose-free therapeutic payload designed to be swallowed whole, minimizing GI distress for adult patients. (Note: 360mg FCT is clinically equivalent to 500mg DT). Excipients (FCT Matrix) Microcrystalline Cellulose / Crospovidone / Povidone K-30 / Poloxamer 188 / Magnesium Stearate / Premium Polymeric Film Diluent / Superdisintegrant / Binder / Solubilizer / Lubricant / Heavy Film-Coating (Engineered specifically utilizing advanced High-Shear Wet Granulation and Poloxamer Solubilization. Because the FCT tablet is highly densified, it requires elite surfactants to guarantee instantaneous release and absorption in the gastrointestinal tract without the need for pre-dispersion) *Pack Sizes: 10×10 Alu-Alu Blisters or Heavy-Gauge HDPE Bottles of 30 (Optimized specifically for strict, 30-day chronic hematology dispensing regimens).
Erythropoietin Prefilled Syringe Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Liquid in a Prefilled Syringe (PFS) with a fine needle.
Active Ingredient Strength (IU) Patient Profile Recombinant Human Erythropoietin 2000 IU / 0.5 ml Maintenance / Low Weight Recombinant Human Erythropoietin 4000 IU / 0.4 ml Standard Dialysis Dose Recombinant Human Erythropoietin 10000 IU / 1.0 ml Chemotherapy / High Dose Stabilizer Human Albumin / Polysorbate Prevents Protein Aggregation *Pack Sizes: Blister Pack of 1 PFS or Box of 6 PFS.
Gabapentin and Methylcobalamin Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Photostable FDC Tablet, packed exclusively in highly secure, light-blocking Alu-Alu blister strips to ensure the absolute chemical survival of the ultra-fragile B12 molecule.
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 and stop the shooting pain. Methylcobalamin (Mecobalamin) JP/USP 500 mcg / 1500 mcg The Myelin Regenerator (Micro-Dose): The highly potent, biologically active B12 analogue required to stimulate axonal growth and rebuild the damaged myelin sheath. Excipients Microcrystalline Cellulose / Croscarmellose Sodium / Copovidone / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Titanium-Dioxide Film Diluent / Superdisintegrant / Binder / Glidant / Film-Coating (Engineered utilizing strictly segregated blending or Bilayer technology to prevent the massive Gabapentin dose from degrading the microscopic Methylcobalamin, finished with a heavy, opaque film-coat to act as an absolute UV/Light barrier) *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict 3-to-6 month chronic diabetic and neurology dispensing regimens).
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).
