CapsulesCapsules
Schedule H (Prescription Required)Prostate & BPH FormulationsCode: 1872

Tamsulosin Hydrochloride 0.4mg + Tolterodine Tartrate 4mg Extended Release Capsules

Generic Formulation:Tamsulosin Hydrochloride 0.4mg and Tolterodine Tartrate 4mg Extended Release Capsules
Pack Size:10's
Common Commercial Brand Equivalents:Market reference only
Jan Aushadhi MRP
₹75
Brand Estimate*
₹392.14
Estimated Savings:₹317.14 (81% saved)
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*Statutory price across 21,118 listed Kendras
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Clinical Overview

Tamsulosin Hydrochloride (0.4mg) and Tolterodine Tartrate (2mg/4mg Extended Release) Capsules is a fixed-dose combination for men suffering from mixed storage and voiding lower urinary tract symptoms (LUTS). Tamsulosin relieves voiding symptoms (hesitancy, weak stream, straining) via alpha-1A adrenergic blockade, while tolterodine competitively antagonizes muscarinic M2/M3 receptors in the detrusor muscle, abolishing involuntary bladder spasms and relieving storage symptoms (frequency, urgency, nocturia). Indicated for men with BPH and co-existing Overactive Bladder (OAB).

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 1872.Report inaccuracy

Usage Guidelines

Take orally once daily after the same meal (preferably breakfast or dinner) with a glass of water. Swallow capsule whole without opening or crushing.

General Administration Advice: Adhere strictly to the prescribed dosage, frequency, and treatment course. For oral medications, swallow with sufficient water. Never stop antibiotics, psychiatric medications, or antihypertensives abruptly without clinical direction.

Possible Side Effects

Common: Dry mouth, dizziness, abnormal ejaculation, constipation, dyspepsia, blurred vision, fatigue. Rare/Severe: Acute urinary retention (AUR), narrow-angle glaucoma attack, and QT interval prolongation.

*Note: Individual physiological responses vary. While many patients experience few or no side effects, notify your treating physician if adverse reactions persist or if hypersensitivity (angioedema, skin rash, dyspnea) occurs.

Precautions & Warnings

Monitor post-void residual (PVR) urine volume prior to starting therapy; contraindicated if baseline PVR exceeds 150-200 mL due to risk of precipitating acute urinary retention. Contraindicated in gastric retention, toxic megacolon, and uncontrolled narrow-angle glaucoma.

Schedule H (Prescription Required)

This medication is scheduled under statutory drug regulatory frameworks (CDSCO / Drugs & Cosmetics Rules). Dispensing requires a valid medical prescription from a registered medical practitioner. Self-medication or unsupervised dosage adjustment carries significant clinical risks.

Medical Disclaimer: Statutory Clinical Disclaimer: The information provided is for educational and price-transparency purposes only and does not constitute medical advice, nephrological diagnosis, or urological treatment recommendations. Always consult a registered nephrologist, urologist, or qualified medical practitioner before initiating, modifying, or discontinuing any kidney or urinary tract medication.