Showing all 8 results

  • Isosorbide Mononitrate Tablets

    Free

    Product 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 IngredientStrength (Standard)Therapeutic Role
    Isosorbide Mononitrate BP/USP20 mgOrganic Nitrate / Vasodilator
    ExcipientsQ.S.Microcrystalline Cellulose / LactoseStabilizing Matrix
  • Isosorbide Tablets

    Free

    Product Composition & Variants

    We supply both Mononitrate and Dinitrate forms in immediate and sustained-release formats.

    Variant TypeStandard StrengthsPrimary Clinical Use
    Isosorbide Mononitrate10mg, 20mg, 40mgProphylaxis: Long-term prevention of angina.
    Isosorbide Dinitrate5mg, 10mg, 20mgAcute & Chronic: Short and long-term heart failure.
    Sustained Release (SR)30mg, 60mgOnce-Daily: For improved patient compliance.
  • Isoxsuprine Tablets

    Free

    Product Composition & Strength

    We supply this product as a Precision-Blended Immediate-Release or Sustained-Release Tablet, packed exclusively in highly secure, moisture-resistant Alu-PVC or Alu-Alu blister strips to ensure the absolute chemical stability of the active pharmaceutical ingredient.

    Active IngredientStrengthPrimary Clinical Function
    Isoxsuprine Hydrochloride USP/Ph.Eur.10 mg (IR)Acute Titration Standard: Immediate-release base unit used for the rapid initiation of therapy or carefully titrated maintenance in sensitive patients.
    Isoxsuprine Hydrochloride USP/Ph.Eur.40 mg (SR)Obstetrics Maintenance Standard: High-efficacy, slow-release matrix designed specifically to provide 12-hour continuous tocolysis, vastly improving maternal compliance and protecting the cardiovascular system.
    ExcipientsHypromellose (HPMC) / Microcrystalline Cellulose / Lactose Monohydrate / Colloidal Silicon Dioxide / Magnesium StearateER Polymer / Diluent / Binder / Glidant / Lubricant (Engineered specifically utilizing premium Hypromellose matrices in the 40mg variant to form a robust hydrogel that slowly erodes in the gastrointestinal tract, ensuring steady-state plasma levels)

    *Pack Sizes: 10×10 Blisters (Optimized specifically for strict obstetric and chronic vascular dispensing regimens).

  • Losartan Potassium, Amlodipine Besylate Tablets

    Free

    Product 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 IngredientStrength (Standard)Therapeutic Role
    Losartan Potassium USP/BP50 mgVasodilator (ARB)
    Amlodipine Besylate USP/BP5 mg (Eq. to Base)Vasodilator (CCB)
    (High Strength Variant)50 mg Losartan + 10 mg Amlodipine
    100 mg Losartan + 5 mg Amlodipine
    Resistant Hypertension
    ExcipientsQ.S.Microcrystalline Cellulose / Sodium Starch GlycolateFiller / Super-Disintegrant
  • Nebivolol Tablets

    Free

    Product Composition & Strength

    We supply this product as a Precision-Blended, Low-Dose 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 IngredientStrengthPrimary Clinical Function
    Nebivolol (as HCl) Ph.Eur./USP2.5 mg / 5 mgGlobal Hypertension Standard: Base therapeutic unit for the continuous, highly tolerated management of essential hypertension.
    Nebivolol (as HCl) Ph.Eur./USP10 mg / 20 mgAdvanced Cardiac Standard: High-dose maintenance therapy for refractory hypertension and specialized heart failure protocols.
    ExcipientsLactose Monohydrate / Microcrystalline Cellulose / Croscarmellose Sodium / Hypromellose / Polysorbate 80 / Magnesium StearateDiluent / Superdisintegrant / Wetting Agent / Lubricant (Engineered specifically to ensure rapid, predictable gastric dissolution while protecting the delicate racemic balance of the API)

    *Pack Sizes: 10×10 Blisters or 28/30-Tablet Calendar Packs (Optimized specifically for strict, high-compliance chronic cardiology dispensing regimens).

  • Nicorandil Tablets

    Free

    Product Composition & Strength

    We supply this product as a Precision-Blended, Moisture-Shielded Tablet, packed exclusively in highly secure, heavy-gauge Alu-Alu blister strips to ensure the absolute chemical stability of the highly volatile active ingredient.

    Active IngredientStrengthPrimary Clinical Function
    Nicorandil Ph.Eur./BP5 mgInitiation / Titration Standard: Base therapeutic unit for the mandatory slow-titration protocol required to build patient tolerance and prevent severe “nitrate headaches.”
    Nicorandil Ph.Eur./BP10 mg / 20 mgGlobal Cardiology Standard: High-dose adult maintenance therapy for severe, refractory stable angina pectoris.
    ExcipientsMaize Starch / Croscarmellose Sodium / Stearic Acid / MannitolLow-Moisture Diluent / Superdisintegrant / Lubricant (Engineered specifically without hygroscopic binders to guarantee the tablet remains perfectly dry and structurally intact throughout its shelf life)

    *Pack Sizes: 10×10 Alu-Alu Blisters (Optimized specifically for strict chronic cardiology dispensing regimens).

  • Nitroglycerin Injection

    Free

    Product Composition & Strength

    We supply this product as a Sterile Concentrate for Infusion in glass ampoules or vials. (Must be diluted).

    Active IngredientStrengthTotal Content
    Nitroglycerin USP/BP5 mg/ml25 mg (in 5 ml Ampoule)
    Nitroglycerin USP/BP5 mg/ml50 mg (in 10 ml Vial)
    ExcipientsPropylene Glycol / EthanolSolubilizers (Volatile)

    *Pack Sizes: Tray of 5 Ampoules or 10 Vials.

  • Nitroglycerin Tablet

    Free

    Product Composition & Available Strengths

    We supply Nitroglycerin Sublingual Tablets in exact, internationally calibrated low-dose strengths to allow for immediate rescue titration during acute ischemic episodes.

    Active Ingredient Common NameCompendial TitleAvailable StrengthsPrimary Clinical Target
    Nitroglycerin (GTN)Glyceryl Trinitrate IP / BP / USP0.4 mgStandard Rescue Dose: Preferred international standard for immediate acute angina abortion.
    Nitroglycerin (GTN)Glyceryl Trinitrate IP / BP / USP0.5 mgHigh-Threshold Prophylaxis: Calibrated for heavy coronary spasm management or pre-exertion protection.