TabletsTablets
Schedule H (Prescription Required)Orthopedic & Joint CareCode: 2223

Amisulpride Tablets 300mg

Generic Formulation:Amisulpride Tablets IP 300mg
Pack Size:10's
Common Commercial Brand Equivalents:Market reference only
Jan Aushadhi MRP
₹75
Brand Estimate*
₹249.97
Estimated Savings:₹174.97 (70% saved)
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*Statutory price across 21,118 listed Kendras
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Clinical Overview

Amisulpride Tablets (300mg) is a substituted benzamide atypical antipsychotic and dopamine D2/D3 receptor antagonist on the WHO Model List framework. At high doses (300-800 mg), it preferentially blocks postsynaptic dopamine D2 and D3 receptors in the limbic system, controlling positive symptoms of schizophrenia; at low doses (50 mg), it blocks presynaptic dopamine autoreceptors, increasing dopamine release to treat negative symptoms, dysthymia, and somatoform pain. Indicated for acute and chronic schizophrenia, dysthymic disorder, and management of chronic pain syndromes with psychosomatic components.

Active Pharmaceutical Ingredients

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 2223.Report inaccuracy

Usage Guidelines

Take orally once or twice daily with water, with or without food. Doses <=300 mg can be taken once daily. Swallow whole.

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: Hyperprolactinemia (galactorrhea, amenorrhea, gynecomastia), weight gain, insomnia, anxiety, extrapyramidal symptoms (tremor, rigidity). Rare/Severe: QTc interval prolongation, Torsades de Pointes, neuroleptic malignant syndrome, and tardive dyskinesia.

*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

Contraindicated in prolactin-dependent tumors, pheochromocytoma, and concurrent QT-prolonging medications. Dose reduction required in renal impairment. Monitor ECG in patients with cardiovascular risk factors.

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, clinical diagnosis, or analgesic treatment guidance. Always consult a registered physician or orthopedic specialist before taking pain relievers, anti-inflammatory medications, or anti-arthritic therapies.