Showing all 9 results
Diltiazem Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (Immediate Release) or Sustained Release (SR) Tablets (Matrix Technology).
Active Ingredient Strength Formulation Role Diltiazem HCl USP/BP 30 mg Immediate Release Initial Titration / Angina Diltiazem HCl USP/BP 60 mg Immediate Release Standard Maintenance Diltiazem HCl USP/BP 90 mg / 120 mg Sustained Release (SR) Twice Daily Control Excipients Q.S. HPMC (Release Matrix) / Lactose Controlled Diffusion Glyceryl Trinitrate Tablets
FreeProduct Composition & Strength
We supply this product as Sublingual Tablets (Dissolve under tongue) or Sustained Release (SR) Tablets (Swallow whole for prevention).
Active Ingredient Strength Formulation Role Diluted Glyceryl Trinitrate USP 0.5 mg (500 mcg) Sublingual (SL) Acute Attack Rescue Diluted Glyceryl Trinitrate USP 2.6 mg Sustained Release (SR) Angina Prophylaxis Diluted Glyceryl Trinitrate USP 6.4 mg Sustained Release (SR) High Dose Maintenance Excipients Q.S. Lactose (Adsorbent) / Stearates Stability Matrixt Isosorbide Mononitrate Tablets
FreeProduct Composition & Strength
We supply this product as Immediate Release Tablets (20 mg). We also offer Extended Release (ER/SR) variants for once-daily dosing through our contract manufacturing division.
Active Ingredient Strength (Standard) Therapeutic Role Isosorbide Mononitrate BP/USP 20 mg Organic Nitrate / Vasodilator Excipients Q.S. Microcrystalline Cellulose / Lactose Stabilizing Matrix Isosorbide Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (Oral) or Sublingual Tablets (Dissolve under tongue).
Active Ingredient Strength Route / Type Role Isosorbide Dinitrate USP/BP 5 mg Sublingual (SL)/ regular Acute Angina Attack Isosorbide Dinitrate USP/BP 10 mg Oral (Swallow) Angina Prophylaxis Isosorbide Dinitrate USP/BP 20 mg Oral (Swallow) Heart Failure / Maintenance Excipients Q.S. Lactose (Diluent) Safety / Bulk Ivabradine 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 blister strips to ensure the absolute chemical stability of the highly hygroscopic hydrochloride salt.
Active Ingredient Strength Primary Clinical Function Ivabradine (as Hydrochloride) USP/Ph.Eur. 5 mg Initiation / Titration Standard: Base therapeutic unit utilized twice daily for the safe initiation of therapy, allowing the cardiologist to monitor resting heart rate before upward titration. Ivabradine (as Hydrochloride) USP/Ph.Eur. 7.5 mg Global Maintenance Standard: High-efficacy adult maintenance dose to strictly maintain the resting heart rate between 50 and 60 beats per minute. Excipients Lactose Monohydrate / Maize Starch / Maltodextrin / Colloidal Silicon Dioxide / Magnesium Stearate / Premium Opadry Film Diluent / Binder / Glidant / Lubricant / Film-Coating (Engineered specifically using precise geometric dilution to ensure the micro-dose API is flawlessly distributed, preventing accidental bradycardia from “hot spots” in a poorly blended generic tablet) *Pack Sizes: 10×10 Blisters or Bottles of 56 (Optimized specifically for strict 28-day chronic cardiology dispensing regimens).
Nifedipine Tablet
FreeProduct Composition & Structural Formats
We supply Nifedipine in exact, internationally standardized strengths, optimized for immediate-release emergency titration or controlled-release daily maintenance.
Active Ingredient Available Strengths Formulation Mechanism Primary Clinical Target Nifedipine IP / BP / USP 10 mg Immediate or Modified Release Acute Titration / Tocolysis: For rapid blood pressure adjustment or suppression of premature labor. Nifedipine IP / BP / USP 20 mg Sustained / Retard Matrix Daily Maintenance: Continuous 12-to-24-hour plasma concentration for chronic hypertension and angina. Nitroglycerin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Concentrate for Infusion in glass ampoules or vials. (Must be diluted).
Active Ingredient Strength Total Content Nitroglycerin USP/BP 5 mg/ml 25 mg (in 5 ml Ampoule) Nitroglycerin USP/BP 5 mg/ml 50 mg (in 10 ml Vial) Excipients Propylene Glycol / Ethanol Solubilizers (Volatile) *Pack Sizes: Tray of 5 Ampoules or 10 Vials.
Telmisartan & Metoprolol Succinate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of both the hygroscopic ARB and the kinetic polymer matrix.
Active Ingredient Strength Primary Clinical Function Telmisartan USP/Ph.Eur. 50 mg Custom-titrated ARB dose for continuous 24-hour peripheral vasodilation and RAAS blockade. Metoprolol Succinate USP/Ph.Eur. 40 mg (Enteric-Coated / ER) Cardioselective beta-1 blockade for continuous heart rate control and anti-anginal defense. Excipients Meglumine / Methacrylic Acid Copolymer (Enteric Coat) / Microcrystalline Cellulose Alkalizer for Telmisartan / Gastric-resistant polymer for Metoprolol (Engineered for strict kinetic segregation) Verapamil Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated Tablets (Immediate Release) or Film Coated Tablets (Sustained Release – SR).
Active Ingredient Strength (Standard) Therapeutic Role Verapamil HCl USP/BP 40 mg / 80 mg Immediate Release (Arrhythmia) Verapamil HCl USP/BP 120 mg (SR) Sustained Release (Hypertension) Verapamil HCl USP/BP 240 mg (SR) High Dose / Once Daily Excipients Q.S. Sodium Alginate / HPMC SR Matrix Former
