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Buprenorphine Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Compressed Sublingual Tablet, engineered for rapid mucosal absorption.
Active Ingredient Strength Primary Clinical Function Buprenorphine HCl USP/Ph.Eur. 0.4 mg / 2 mg The Pain & Induction Anchor: Low-dose format for chronic pain or the initial phase of addiction treatment. Buprenorphine HCl USP/Ph.Eur. 8 mg The Maintenance Payload: High-strength dose for long-term stabilization in Opioid Use Disorder. Excipients Sublingual Matrix Rapid Dissolution System: Engineered to dissolve completely under the tongue in < 2 minutes for maximum transmucosal bioavailability. Morphine Sulphate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Extended-Release Matrix Tablet, packed exclusively in highly secure, tamper-evident Alu-PVC or Alu-Alu blister strips to ensure the absolute physical stability of the controlled-release polymers.
Active Ingredient Strength Primary Clinical Function Morphine Sulphate USP/Ph.Eur. 15 mg (SR) Initiation / Titration Standard: Base therapeutic unit for opioid-naïve patients starting around-the-clock chronic pain management. Morphine Sulphate USP/Ph.Eur. 30 mg / 60 mg (SR) Global Oncology Standard: High-dose adult maintenance therapy for severe, opioid-tolerant terminal cancer and intractable neuropathic pain. Excipients Hypromellose (HPMC) / Cetostearyl Alcohol / Lactose Monohydrate / Magnesium Stearate / Premium Color-Coded Film Hydrophilic Polymer / Lipophilic Retardant / Diluent / Lubricant (Engineered specifically to form an impenetrable, slow-eroding gel matrix in the GI tract, strictly metering the release of the narcotic over 12 hours) *Pack Sizes: 10×10 Blisters (Optimized specifically for strict 30-day chronic oncology dispensing regimens; frequently color-coded by strength to prevent fatal dispensing errors).
