Generic Verampil (Verapamil HCl)

Verampil
Verampil is a calcium channel blocker prescribed in treatment of hypertension, angina, and certain heart rhythm disorders.
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Introduction

Verampil is a generic oral formulation that contains the active compound Verapamil HCl. It belongs to the class of calcium-channel blockers, specifically the phenylalkylamine subclass. The medication is available in 40 mg and 120 mg tablets. Verampil is primarily indicated for the management of hypertension, chronic stable angina, and certain cardiac arrhythmias such as supraventricular tachycardia (SVT) and atrial fibrillation with rapid ventricular response. In clinical practice, it is also used for hypertrophic cardiomyopathy and, in some settings, for migraine prophylaxis and other off-label purposes.

What is Verampil?

  • Definition: Verampil is the generic version of well-known medications, containing the active compound Verapamil HCl. Our online pharmacy provides this generic alternative as a cost-effective treatment option.
  • Classification: It is a phenylalkylamine calcium-channel blocker (CCB).
  • Development history: Verapamil was first synthesized in the early s and received regulatory approval for cardiovascular use in 1981. The generic market expanded after patent expiration, allowing formulations such as Verampil to be produced by multiple manufacturers worldwide.
  • Manufacturer: The specific manufacturer of Verampil may vary; however, all tablets supplied through our pharmacy are sourced from licensed, GMP-certified suppliers.
  • Brand equivalents: Verapamil HCl is marketed under brand names such as Isoptin, Verelan, and Calan.

How Verampil Works

Verapamil blocks L-type voltage-gated calcium channels located on the membranes of cardiac myocytes, vascular smooth-muscle cells, and the conduction tissue of the heart. By inhibiting calcium influx:

  1. Vascular smooth muscle relaxation reduces systemic arterial resistance, lowering blood pressure.
  2. Negative inotropy diminishes myocardial contractility, decreasing myocardial oxygen demand and relieving angina.
  3. AV-node conduction slowing slows impulse propagation through the atrioventricular node, helping control ventricular rate in supraventricular tachyarrhythmias.

The onset of action after oral administration occurs within 1-2 hours, with peak plasma concentrations at 2-4 hours. The elimination half-life ranges from 3 to 7 hours, allowing twice-daily dosing for most indications. Verapamil is metabolized primarily by hepatic CYP3A4 and excreted renally as unchanged drug and metabolites.

Conditions Treated with Verampil

Approved indication Why Verampil is effective
Hypertension Reduces systemic vascular resistance through arterial smooth-muscle relaxation, providing steady blood-pressure control.
Chronic stable angina Lowers myocardial oxygen consumption by decreasing contractility and heart rate, while improving coronary blood flow via vasodilation.
Supraventricular tachycardia (SVT) Prolongs AV-node refractory period, interrupting re-entrant circuits that cause rapid heart rates.
Rate control in atrial fibrillation Slows ventricular response by inhibiting calcium-dependent conduction through the AV node, improving hemodynamics.
Hypertrophic obstructive cardiomyopathy (HOCM) Decreases left-ventricular outflow tract gradients by reducing contractility and improving diastolic filling.

Each of these uses is supported by large-scale clinical trials and regulatory approval from agencies such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA).

Off-Label and Investigational Uses of Verampil

  • Migraine prophylaxis - Small randomized trials have shown that verapamil can reduce migraine frequency, likely through modulation of cerebral vasculature. This use is not approved by regulatory bodies.
  • Cluster headache - Case series suggest benefit in refractory cluster headache, attributed to central analgesic mechanisms. Evidence remains limited.
  • Hypertensive emergencies (intravenous formulation) - While the oral tablet is not indicated, the IV version of verapamil is sometimes employed in acute settings under strict monitoring.
  • Anxiety disorders - Some pilot studies report anxiolytic effects via attenuation of autonomic over-activity, but data are preliminary.

Important: Off-label applications have not undergone the rigorous evaluation required for official approval. Patients should discuss any such use with a qualified healthcare provider, and therapy should only be initiated under professional supervision.

Is Verampil the Right Medication for You?

Verampil is appropriate for adults who require pharmacologic control of:

  • Mild-to-moderate essential hypertension when first-line therapy is insufficient or contraindicated.
  • Symptomatic chronic angina unresponsive to beta-blockers or nitrates.
  • Documented supraventricular tachyarrhythmias where rate control or rhythm conversion is needed.
  • Hypertrophic obstructive cardiomyopathy with outflow-tract obstruction.

Contraindications and cautions

  • Severe hypotension (systolic < 90 mmHg) or cardiogenic shock.
  • Advanced heart block (second- or third-degree AV block) without a permanent pacemaker.
  • Sick sinus syndrome.
  • Recent myocardial infarction (within 48 hours) or acute decompensated heart failure.
  • Known hypersensitivity to verapamil or other phenylalkylamine CCBs.
  • Pregnant or breastfeeding women should use only if the potential benefit justifies the potential risk; verapamil crosses the placenta and is excreted in milk.

Patients with hepatic impairment, renal dysfunction, or concurrent use of strong CYP3A4 inhibitors require dose adjustments or close monitoring.

Risks, Side Effects, and Interactions

Common (≥1 % incidence)

  • Constipation
  • Dizziness or light-headedness, especially on standing (orthostatic hypotension)
  • Headache
  • Peripheral edema (ankle swelling)
  • Nausea / abdominal discomfort

Rare (.1 %-1 % incidence)

  • Bradycardia (HR < 50 bpm)
  • AV-node block (first-degree)
  • Gingival hyperplasia (particularly with long-term use)
  • Visual disturbances (blurred vision)

Serious (≤.1 % incidence)

  • Severe hypotension leading to syncope
  • High-grade AV block or complete heart block (may require pacemaker)
  • Acute heart failure exacerbation
  • Myocardial depression in patients with pre-existing left-ventricular dysfunction
  • Fatal arrhythmias when combined with certain anti-arrhythmic agents

Drug-Drug Interactions

  • Beta-blockers (e.g., metoprolol): additive negative chronotropic effects → increased bradycardia risk.
  • Digoxin: verapamil raises digoxin serum concentrations; monitor for digoxin toxicity.
  • CYP3A4 inhibitors (ketoconazole, clarithromycin, itraconazole, grapefruit juice): increase verapamil plasma levels → heightened adverse-event risk.
  • CYP3A4 inducers (rifampin, carbamazepine, phenytoin, St. John’s wort): reduce plasma concentrations → loss of efficacy.
  • Other calcium-channel blockers (diltiazem, amlodipine): additive vasodilatory effects → profound hypotension.

Drug-Food Interactions

  • Grapefruit and grapefruit juice markedly inhibit intestinal CYP3A4, raising verapamil concentrations. Patients should avoid large quantities of grapefruit products.

Use: Dosing, Missed Dose, Overdose

Standard dosing ranges (oral tablets)

Indication Starting dose Typical maintenance dose Frequency
Hypertension 80 mg once daily 120-240 mg daily (may be divided) 1-2 × daily
Chronic angina 80 mg once daily 120-480 mg daily 1-3 × daily
SVT / A-fib rate control 80 mg twice daily 180-240 mg twice daily 2 × daily
Hypertrophic cardiomyopathy 40 mg three times daily 120 mg three times daily 3 × daily

Dose titration is performed at intervals of 1-2 weeks based on blood-pressure response, angina frequency, and heart-rate control.

Missed dose If a dose is missed and the next scheduled dose is more than 6 hours away, take the missed tablet as soon as remembered. If the time for the next dose is less than 6 hours away, skip the missed dose and resume the regular schedule. Do not double-dose.

Overdose Signs of verapamil overdose include profound hypotension, bradycardia, AV block, cardiac arrest, and seizures. Management is supportive and may require:

  • Immediate medical attention in an emergency department.
  • Intravenous fluids, vasopressors (e.g., norepinephrine), and atropine or glucagon for bradycardia.
  • Calcium gluconate infusion to counteract calcium-channel blockade.
  • Activated charcoal if ingestion occurred within 1 hour and the patient is alert.

Prompt professional care is essential; overdose can be life-threatening.

FAQ

  • What does a Verampil tablet look like?   Verampil tablets are oval, film-coated, and color-coded by strength: the 40 mg tablet is white, while the 120 mg tablet is pink. Imprint markings identify the manufacturer and dosage.

  • Can I travel internationally with Verampil?   Yes. Carry the medication in its original container, keep a copy of the prescription (or a physician’s note for personal use), and verify import regulations of the destination country. Some jurisdictions may require a customs declaration for bulk quantities.

  • How should Verampil be stored?   Store tablets at room temperature (15-30 °C), away from moisture, heat, and direct sunlight. Keep the bottle tightly closed and out of reach of children. Do not freeze.

  • Does Verampil affect laboratory tests?   Verapamil can modestly lower serum potassium and may interfere with plasma concentrations of digoxin. It does not significantly alter routine liver-function or renal panels, but inform the laboratory of ongoing therapy if unusual results occur.

  • Is Verampil safe during pregnancy?   Animal studies have not shown teratogenicity, but human data are limited. Verapamil is classified as FDA pregnancy category C; it should be used only if the potential maternal benefit outweighs possible fetal risk. Consultation with a maternal-fetal specialist is recommended.

  • Can I breastfeed while taking Verampil?   Verapamil is excreted in breast milk in small amounts. While no adverse effects have been documented in infants, the decision to breastfeed should be made with a healthcare provider, considering the infant’s health and the mother’s need for blood-pressure control.

  • Will Verampil show up on a drug test?   Verapamil is not a controlled substance and is not screened for in standard occupational drug-testing panels. Specialized toxicology assays could detect it, but routine employment tests will not flag Verampil.

  • How does Verampil differ from other calcium-channel blockers such as amlodipine?   Verapamil predominantly affects cardiac conduction and contractility, making it useful for arrhythmia control. Amlodipine, a dihydropyridine CCB, mainly causes peripheral vasodilation with minimal cardiac effects, making it better suited for isolated hypertension.

  • What is the historical significance of verapamil’s discovery?   Verapamil was discovered by scientists at Ortho-Pharma in the early s as part of a series of phenylalkylamine compounds aimed at selective cardiac effects. Its approval in 1981 represented the first calcium-channel blocker with strong negative-inotropic and AV-node-blocking properties, expanding therapeutic options beyond beta-blockers.

  • Does taking Verampil influence exercise capacity?   By reducing heart-rate and myocardial oxygen demand, verapamil may modestly lower maximal exercise tolerance, especially in high-intensity activities. Patients should monitor symptoms and adjust activity levels under medical guidance.

Glossary

L-type calcium channel
A voltage-gated channel primarily responsible for calcium influx in cardiac and smooth-muscle cells; blockade reduces contraction strength and vascular tone.
Negative inotropy
Decrease in the strength of cardiac muscle contraction, leading to reduced stroke volume and oxygen consumption.
AV-node refractory period
The time during which the atrioventricular node cannot conduct another impulse; prolongation slows ventricular response in tachyarrhythmias.
CYP3A4
A liver enzyme that metabolizes many drugs; inhibitors raise drug levels, while inducers lower them.

Buying Verampil from Our Online Pharmacy

Patients who need affordable, high-quality verapamil often encounter price barriers or limited local availability. Our online pharmacy offers Verampil at a price that approaches the manufacturer’s cost, providing a genuine cost-saving opportunity without compromising safety.

All tablets are sourced from licensed, GMP-certified overseas pharmacies that adhere to rigorous quality-control standards. Before shipment, each batch undergoes independent verification to confirm potency, purity, and proper labeling.

We guarantee discreet packaging and reliable delivery-express service typically arrives within 7 days, while standard airmail takes 2-3 weeks, depending on the destination. Because we act as a pharmacy-broker service, we can source medications that may be unavailable through domestic retail channels, ensuring continuity of care for patients in remote or underserved regions.

Your privacy is paramount. Orders are processed with secure encryption, and no identifying information appears on the exterior of the package. In this way, we combine affordability, safety, and discretion to help you obtain the medication you need.

Disclaimer

The information presented about Verampil is intended for general educational purposes and does not replace professional medical advice. Treatment decisions-including considerations of off-label use-should be made under the direct supervision of a qualified healthcare provider. Readers are assumed to be responsible adults capable of making informed health choices. Our online pharmacy supplies Verampil to individuals who may encounter limited access through conventional pharmacies or insurance plans, or who are seeking affordable generic alternatives. Always consult a qualified clinician before initiating, adjusting, or stopping any medication.

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