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Adrenaline Injections
FreeProduct Composition & Strength
We supply this product as a Sterile Solution in Amber Glass Ampoules. The formulation includes stabilizers to prevent rapid oxidation.
Active Ingredient Strength (Standard 1:1000) Therapeutic Role Adrenaline Bitartrate BP/USP Eq. to Adrenaline 1 mg / ml Vasopressor / Bronchodilator Excipients Q.S. Sodium Metabisulfite / Sodium Chloride Antioxidant / Isotonicity *Pack Sizes: Tray of 10 Ampoules (1ml each) or Box of 50/100 Ampoules (Hospital Pack).
Amlodipine & Enalapril Maleate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets to protect the Enalapril Maleate from moisture-induced degradation and to ensure the physical integrity of the combination.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine (as Besylate) BP/USP 5 mg / 10 mg Calcium Channel Blocker (CCB) Enalapril Maleate BP/USP 5 mg / 10 mg / 20 mg ACE Inhibitor Excipients Q.S. Sodium Stearyl Fumarate / Lactose Lubricant & Stabilizer Amlodipine & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, engineered for synchronized 24-hour hemodynamic control.
Active Ingredient Strength Primary Clinical Function Amlodipine (as Besylate) USP/BP 5 mg / 10 mg The Vasodilator: Reduces the resistance of blood vessels to lower systemic pressure. Hydrochlorothiazide USP/BP 12.5 mg / 25 mg The Volume Reducer: Excretes excess sodium and water to reduce circulatory load. Excipients Proprietary Matrix Steady-State System: Engineered to ensure consistent plasma concentrations of both drugs to prevent “dips” in BP control. Amlodipine Besylate & Losartan Potassium Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The formulation is optimized for 24-hour efficacy, allowing for convenient once-daily dosing.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine Besylate BP/USP 5 mg Calcium Channel Blocker (CCB) Losartan Potassium BP/USP 50 mg Angiotensin Receptor Blocker (ARB) Excipients Q.S. Microcrystalline Cellulose / Starch Stabilizing Core Matrix Amlodipine Tablet
FreeAmlodipine Tablets IP 5 mg
Each Uncoated tablet contains :
Amlodipine Besylate IP
Eq to Amlodipine 5 mgAmlodipine Tablets IP 10 mg
Each Uncoated Tablet Contains :
Amlodipine Besylate IP
Eq To Amlodipine 10 mgAmlodipine Besylate Tablets IP 2.5 mg
Each uncoated tablet contains :
Amlodipine Besylate IP
Eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 2.5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 2.5 mgAmlodipine Besylate Tablets IP 5 mg
Each Film Coated Tablet Contains:
Amlodipine Besylate IP
eq. To Amlodipine 5 mgAMLODIPINE & ENALAPRIL MALEATE TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Enalapril Maleate 5 mg
Excipients q.sAMLODIPINE & LISINOPRIL TABLET
Each Film Coated Tablet Contains :
Amlodipine Besylate
Eq. To Amlodipine 5 mg
Lisinopril dihydrate
Eq. To Lisinopril 5 mg
Excipients q.sTRIPPLEACE AMLODIPINE -10 / AMLODIPINE
TABLETS 10 MG
Each uncoated tablet contains:
Amlodipine Besilate BP
Equivalent to Amlodipine 10 mg
Excipients Q.S.Usage: – Treat high blood pressure
Category: – Hypertensive / Cardiac Drugs
Therapeutic category: – hypertensive, Cardiovascular Agent,
Amlodipine With Lisinopril Dehydrate Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets. The use of Lisinopril in its Dihydrate form ensures superior stability and predictable dissolution profiles.
Active Ingredient Strength (Standard) Therapeutic Role Amlodipine (as Besylate) BP/USP 5 mg / 10 mg Calcium Channel Blocker Lisinopril (as Dihydrate) BP/USP 5 mg / 10 mg / 20 mg ACE Inhibitor Excipients Q.S. Calcium Phosphate / Mannitol Stabilizing Agents Atenolol & Chlorthalidone Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The combination is engineered to maintain therapeutic plasma levels over a 24-hour period, supporting once-daily dosing.
Active Ingredient Strength (Standard) Therapeutic Role Atenolol BP/USP 50 mg / 100 mg Cardioselective Beta-Blocker Chlorthalidone BP/USP 12.5 mg / 25 mg Long-acting Diuretic Excipients Q.S. Magnesium Stearate / Povidone Stabilizing Core Matrix Atenolol & Indapamide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, engineered for synchronized 24-hour hemodynamic control.
Active Ingredient Strength Primary Clinical Function Atenolol USP/BP 50 mg The Heart Rate Regulator: Controls cardiac output and myocardial oxygen demand. Indapamide USP/BP 2.5 mg The Metabolic-Neutral Diuretic: Reduces blood volume and provides direct vascular relaxation. Excipients Proprietary Matrix Steady-State Release System: Engineered to ensure consistent plasma concentrations of both drugs to prevent “dips” in BP control. Atenolol & S-Amlodipine Besylate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended, Film-Coated Tablet, utilizing high-purity S-Amlodipine Besylate to ensure stability.
Active Ingredient Strength Primary Clinical Function Atenolol USP/BP 25 mg / 50 mg The Heart Rate Regulator: Controls the “Pump” by reducing heart rate and myocardial oxygen demand. S-Amlodipine (as Besylate) USP/BP 2.5 mg / 5 mg The Vessel Relaxant: Pure chiral isomer for maximum vasodilation with minimum side effects (edema). Excipients Proprietary Matrix Chiral-Stability System: Engineered to ensure the S-enantiomer remains stable and does not racemize during the shelf-life. Atenolol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated or Film Coated Tablets (often scored for dosage adjustment).
Active Ingredient Strength (Standard) Role Atenolol IP/BP/USP 25 mg Low Dose / Renal Impairment Atenolol IP/BP/USP 50 mg Standard Adult Dose Atenolol IP/BP/USP 100 mg High Potency / Angina Excipients Q.S. Binder / Disintegrant Atorvastatin Clopidogrel and Aspirin Capsules
FreeAtorvastatin, clopidogrel, and aspirin capsules are fixed-dose combination (FDC) medications used for the secondary prevention of cardiovascular events like heart attacks and strokes.
Atorvastatin Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. The active ingredient is used in the amorphous or crystalline form depending on bioavailability requirements.
Active Ingredient Strength (Standard) Role Atorvastatin Calcium IP/BP/USP 10 mg Primary Prevention / Maintenance Atorvastatin Calcium IP/BP/USP 20 mg Standard Therapeutic Dose Atorvastatin Calcium IP/BP/USP 40 mg High Intensity Therapy Atorvastatin Calcium IP/BP/USP 80 mg Acute Coronary Syndrome Bisoprolol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (distinctively shaped/scored). The low-dose range is critical for the “Start Low, Go Slow” titration required in heart failure.
Active Ingredient Strength (Standard) Shape/Color Primary Role Bisoprolol Fumarate USP/BP 2.5 mg White (Scored) Heart Failure Initiation Bisoprolol Fumarate USP/BP 5 mg Yellow/Pink (Scored) Standard Hypertension Bisoprolol Fumarate USP/BP 10 mg Orange/White High Dose Maintenance Excipients Q.S. Microcrystalline Cellulose / Hypromellose Filler / Coating Candesartan Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored). The wide range of strengths allows for precise titration in heart failure patients.
Active Ingredient Strength (Standard) Primary Role Candesartan Cilexetil USP/BP 4 mg Heart Failure Initiation / Hepatic Impairment Candesartan Cilexetil USP/BP 8 mg Standard Hypertension Start Candesartan Cilexetil USP/BP 16 mg Standard Maintenance Candesartan Cilexetil USP/BP 32 mg High Dose / Resistant Hypertension Carvedilol Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets. Because therapy for Heart Failure requires very precise “low dose” initiation, we offer the full titration range.
Active Ingredient Strength (Standard) Color Code (Typical) Role Carvedilol USP/BP 3.125 mg White/Pink CHF Initiation (Critical) Carvedilol USP/BP 6.25 mg Yellow Titration Step 1 Carvedilol USP/BP 12.5 mg Tan/Peach Titration Step 2 Carvedilol USP/BP 25 mg White Target Maintenance Dose Cilostazol Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (White, circular). Precise formulation is required to manage its solubility profile.
Active Ingredient Strength (Standard) Primary Role Cilostazol USP/BP 50 mg Initiation / Renal Adjustment Cilostazol USP/BP 100 mg Standard Maintenance Dose Excipients Q.S. Microcrystalline Cellulose / CMC Calcium 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 Enalapril Tablets
FreeProduct Composition & Strength
We supply this product as Uncoated Tablets (scored for titration). The wide range of strengths allows for the “Start Low, Go Slow” dosing strategy essential for heart failure.
Active Ingredient Strength (Standard) Primary Role Enalapril Maleate USP/BP 2.5 mg Heart Failure Initiation Enalapril Maleate USP/BP 5 mg Hypertension Initiation Enalapril Maleate USP/BP 10 mg Maintenance Dose Enalapril Maleate USP/BP 20 mg High Strength Hydralazine Tablets
FreeProduct Composition & Strength
We supply this product as Sugar Coated or Film Coated Tablets (often Yellow or Orange). Uncoated tablets are avoided due to stability issues.
Active Ingredient Strength (Standard) Role Hydralazine HCl USP/BP 25 mg Initial Dose / Titration Hydralazine HCl USP/BP 50 mg Maintenance Dose Excipients Q.S. Coating Agents / Stabilizers Losartan Potassium, Amlodipine Besylate Tablets
FreeProduct Composition & Strength
We supply this product as Film Coated Tablets (typically White or Yellow, Oval/Round). The formulation uses the Besylate salt of Amlodipine for maximum stability.
Active Ingredient Strength (Standard) Therapeutic Role Losartan Potassium USP/BP 50 mg Vasodilator (ARB) Amlodipine Besylate USP/BP 5 mg (Eq. to Base) Vasodilator (CCB) (High Strength Variant) 50 mg Losartan + 10 mg Amlodipine
100 mg Losartan + 5 mg AmlodipineResistant Hypertension Excipients Q.S. Microcrystalline Cellulose / Sodium Starch Glycolate Filler / Super-Disintegrant Losartan Tablet
FreeProduct Composition & Available Strengths
We supply Losartan Potassium across the complete, internationally recognized therapeutic range to facilitate progressive dose titrations and precise maintenance regimens.
Active Ingredient Monograph Available Strengths Formulation Matrix Delivery System Primary Clinical Application Losartan Potassium USP / BP / IP 25 mg Oral Solid Film-Coated Tablet Pediatric & Low-Dose Titration: For introductory pediatric hypertension care or initial combination-therapy building. Losartan Potassium USP / BP / IP 50 mg Oral Solid Film-Coated Tablet Core Commercial Volume: Standard international baseline daily dose for mild-to-moderate chronic essential hypertension. Losartan Potassium USP / BP / IP 100 mg Oral High-Potency Solid Tablet Maximal Saturation Maintenance: For advanced hypertensive management, diabetic nephropathy progression delay, and stroke risk reduction in left ventricular hypertrophy. Metoprolol Tablet
FreeCore Product Catalog:
Active Ingredient Monograph Standard Strengths Dosage Format Primary Clinical Target Metoprolol Tartrate IP/BP/USP 25 mg Immediate-Release Solid Tablet Acute Titration: For fine-tuned early adjustment in arrhythmias and mild hypertension. Metoprolol Tartrate IP/BP/USP 50 mg Immediate-Release Solid Tablet Standard Twice-Daily Blockade: Routine maintenance for Angina Pectoris and post-Myocardial Infarction stabilization. Metoprolol Tartrate IP/BP/USP 100 mg Immediate-Release Solid Tablet High-Threshold Control: For refractory tachyarrhythmias and intensive post-MI clinical management. Ramipril & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Film-Coated Tablet or Capsule, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly degradable Ramipril molecule.
Active Ingredient Strength Primary Clinical Function Ramipril Ph.Eur./USP 5 mg (or 2.5 mg / 10 mg) ACE inhibition for vasodilation, RAAS blockade, and critical potassium retention. Hydrochlorothiazide Ph.Eur./USP 12.5 mg / 25 mg Global Clinical Standard: Thiazide diuretic for sodium excretion and sustained blood volume reduction. Excipients Microcrystalline Cellulose / Sodium Starch Glycolate / Sodium Bicarbonate / Hypromellose / Magnesium Stearate Diluent / Superdisintegrant / Alkaline Stabilizing Agent (Engineered specifically to protect Ramipril from acidic degradation and moisture-induced cyclization) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for strict, high-compliance 30-day chronic cardiology dispensing regimens).
Ramipril Tablets
FreeRamipril Tablets IP 2.5mg
Each Film coated tablet contains:
Ramipril IP 2.5 mgRamipril tablets IP 5 mg
Each Filmcoated tablet contains :
Ramipril IP 5 mgUsage: – high blood pressure and heart failure
Category: – Anti Cardiovascular drugs
Therapeutic category: – Cardiovascular Agent, Antihypertensive
Pcd marketing:-
Manufacturer: – Healthy Life Pharma Pvt Ltd
Exporter: – Healthy Inc
Supplier: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Distributor: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Seller: – Healthy Life Pharma Pvt Ltd
Healthy Inc
Rosuvastatin & Clopidogrel Capsules
FreeRosuvastatin and clopidogrel capsules are fixed-dose combination (FDC) medications used for the secondary prevention of cardiovascular events like heart attacks and strokes. They are typically available in strengths such as 10 mg/75 mg or 20 mg/75 mg.
Rosuvastatin & Fenofibrate Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Bilayer or Matrix Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute chemical stability of the highly sensitive Rosuvastatin calcium salt.
Active Ingredient Strength Primary Clinical Function Rosuvastatin Calcium INN/Ph.Eur. 10 mg or 20 mg (Equivalent to Rosuvastatin base) Potent HMG-CoA Reductase inhibition for massive LDL reduction and plaque stabilization. Fenofibrate (Micronized) INN/Ph.Eur. 160 mg (or 145 mg Nanoparticle) Global Clinical Standard: PPAR-alpha agonism for severe hypertriglyceridemia and HDL elevation. Excipients Lactose Monohydrate / Sodium Lauryl Sulfate / Crospovidone / Magnesium Stearate Diluent / Surfactant / Superdisintegrant (Engineered with heavy surfactant loading to force the insoluble Fenofibrate into systemic circulation) *Pack Sizes: 10×10 Alu-Alu Blisters or 3×10 Unit-Dose Blisters (Optimized specifically for high-compliance 30-day chronic cardiology dispensing regimens).
Rosuvastatin Clopidogrel and Aspirin Capsules
FreeRosuvastatin, clopidogrel, and aspirin capsules are fixed-dose combination (FDC) medications used for the prevention of serious cardiovascular events such as heart attacks and strokes. This “triple therapy” combines a cholesterol-lowering statin with two antiplatelet agents
Telmisartan & Chlorthalidone Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Blended Bilayer or Matrix 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 micro-dosed diuretic.
Active Ingredient Strength Primary Clinical Function Telmisartan USP/Ph.Eur. 40 mg Standard ARB maintenance dose for continuous 24-hour peripheral vasodilation and RAAS blockade. Chlorthalidone USP/Ph.Eur. 6.25 mg Highly precise, long-acting thiazide-like diuresis optimized for maximum safety and efficacy. Excipients Meglumine / Sodium Hydroxide / Microcrystalline Cellulose / Sodium Starch Glycolate Alkalizer for Telmisartan / Diluent / Superdisintegrant (Engineered for kinetic segregation and immediate dissolution) 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) Telmisartan & Metoprolol 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. 40 mg Standard ARB maintenance dose for continuous 24-hour peripheral vasodilation. Metoprolol Succinate USP/Ph.Eur. 25 mg (Extended-Release) Low-dose cardioselective beta-1 blockade for gentle heart rate control and initiation therapy. Excipients Meglumine / Hypromellose (HPMC) / Microcrystalline Cellulose / Sodium Hydroxide Alkalizer for Telmisartan / SR Polymer matrix for Metoprolol (Engineered for kinetic segregation) Telmisartan 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. The formulation utilizes specialized alkalizing agents to ensure the highly insoluble API rapidly dissolves in the gastrointestinal tract.
Active Ingredient Strength Primary Clinical Use Telmisartan USP/BP/Ph.Eur. 20 mg Initiation / Hepatic Impairment: Low-dose titration for sensitive or hepatically compromised patients. Telmisartan USP/BP/Ph.Eur. 40 mg Standard Global Dose: Once-daily maintenance therapy for essential hypertension. Telmisartan USP/BP/Ph.Eur. 80 mg Maximum CV Protection: High-dose therapy for severe hypertension and mandated cardiovascular risk reduction. Excipients Meglumine / Sodium Hydroxide / Povidone / Magnesium Stearate Alkalizing Stabilizer / Binder / Lubricant (Engineered to prevent API crystallization and ensure rapid absorption) Telmisartan, Amlodipine & Hydrochlorothiazide Tablets
FreeProduct Composition & Strength
We supply this product as a Precision-Engineered Multi-Layer or Segregated Matrix Film-Coated Tablet, packed exclusively in highly secure, moisture-resistant Alu-Alu blister strips to ensure the absolute stability of the hygroscopic ARB and the sensitive CCB.
Active Ingredient Strength Primary Clinical Function Telmisartan USP/Ph.Eur. 40 mg Continuous 24-hour peripheral vasodilation and potassium-sparing RAAS blockade. Amlodipine Besylate USP/Ph.Eur. 5 mg (Equivalent to Amlodipine base) Calcium channel blockade for direct arterial relaxation and anti-anginal defense. Hydrochlorothiazide (HCTZ) USP/Ph.Eur. 12.5 mg Thiazide diuresis for blood volume reduction and mitigation of peripheral edema. Excipients Meglumine / Microcrystalline Cellulose / Sodium Starch Glycolate / Magnesium Stearate Alkalizer for Telmisartan / Diluent / Superdisintegrant (Engineered for kinetic segregation) *Pack Sizes: 10×10 or 10×15 Alu-Alu Blisters (Optimized specifically for strict 30-day chronic cardiology adherence regimens).
Terlipressin Injection
FreeProduct Composition & Strength
We supply this product as a Sterile Lyophilized Powder (White to Off-White Cake) in glass vials, requiring reconstitution with a provided sterile diluent.
Active Ingredient Strength Reconstitution Requirement Terlipressin (as Acetate) USP/BP 1 mg Requires 5 ml of 0.9% Sodium Chloride Diluent Excipients Mannitol / Glacial Acetic Acid Bulking Agent / pH Adjustment *Pack Sizes: 1 Vial of Lyophilized Powder + 1 Ampoule of Diluent (5 ml) per box.
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
