25 mg Controlled-Release Action
Polymer-coated matrix delivers complete 25 mg paroxetine release in the small intestine, providing maximum SERT occupancy with minimal gastric nausea.
PAXOTIN-CR-FORTE is a high-strength controlled-release neuropsychiatric formulation combining Paroxetine Hydrochloride IP equivalent to Paroxetine 25 mg (CR) with Clonazepam IP 0.5 mg by Blessme, Dellwich Lifescience LLP. Engineered for severe refractory major depressive disorder, debilitating panic disorder with agoraphobia, and severe anxiety states, providing full therapeutic 24-hour serotonergic restoration with immediate GABAergic anti-panic coverage.

Detailed pharmaceutical specifications, active API monograph compliance, full-strength controlled-release matrix synergy, and 10x10 aluminium strip packaging details for PAXOTIN-CR-FORTE.
PAXOTIN-CR-FORTE provides full-strength 25 mg Paroxetine CR paired with 0.5 mg Clonazepam. Formulated for patients suffering from severe depression complicated by frequent panic attacks, intense somatic anxiety, and persistent insomnia requiring maximal therapeutic effect.
In-depth pharmacological evaluation of Paroxetine CR 25 mg + Clonazepam 0.5 mg tablets, marketed as PAXOTIN-CR-FORTE by Blessme (Dellwich Lifescience LLP). Covers full-strength panic control, refractory depression treatment, and pharmaceutical supply across India.
PAXOTIN-CR-FORTE is a full-strength oral neuropsychiatric formulation combining an extended-release enteric formulation of the potent SSRI (Paroxetine CR 25 mg) with a high-affinity positive GABA_A modulator (Clonazepam 0.5 mg).
When patients suffer from severe treatment-resistant depression or debilitating panic disorder with agoraphobia, lower doses may fail to achieve clinical remission. PAXOTIN-CR-FORTE provides the definitive 25 mg maintenance dose with immediate high-potency anxiolytic coverage via Clonazepam from day one.
Approved neurological and psychiatric indications for PAXOTIN-CR-FORTE include:
Paroxetine 25 mg acts as a highly selective and potent inhibitor of the serotonin transporter (SERT). By preventing serotonin reuptake across 24 continuous hours, it steadily elevates synaptic 5-HT concentrations, promoting brain-derived neurotrophic factor (BDNF) expression and reversing stress-induced atrophy in the hippocampus and prefrontal cortex over 2 to 4 weeks.
Simultaneously, Clonazepam 0.5 mg acts immediately as a positive allosteric modulator on the GABAA receptor complex. By increasing chloride influx, it hyperpolarizes limbic neurons, immediately terminating acute panic attacks, motor restlessness, and severe autonomic surges from the very first dose.
Clinical selection criteria between the two strengths:
PAXOTIN-CR-FORTE must be taken strictly in accordance with medical advice:
PAXOTIN-CR-FORTE contains Clonazepam, which carries potential for dependence and habit formation with prolonged therapy. Do not consume alcohol during therapy. Contraindicated with monoamine oxidase inhibitors (MAOIs). Dispensed strictly against a valid medical prescription.
PAXOTIN-CR-FORTE is manufactured in WHO-GMP certified facilities adhering to Schedule M protocols, ensuring micro-blend homogeneity and maximum packaging stability.
Polymer-coated matrix delivers complete 25 mg paroxetine release in the small intestine, providing maximum SERT occupancy with minimal gastric nausea.
Tamper-evident 10x10 aluminium-aluminium foil packaging shields active APIs against atmospheric moisture and thermal degradation for extended shelf stability.
Every batch is verified through authenticated Certificates of Analysis (COA), multi-point dissolution profiling, and HPLC active assay validation complying with IP standards.
Produced in state-of-the-art cleanroom manufacturing units in Gujarat adhering to automated compression, online check-weighing, and Good Laboratory Practices (GLP).
Prescribing guidance, contraindications, and drug interactions for Paroxetine CR 25 mg + Clonazepam 0.5 mg tablets.
PAXOTIN-CR-FORTE is a Schedule H prescription drug. Not for OTC sale. Do not consume alcohol during therapy. Exercise caution when driving or operating machinery.
Approved neurological and psychiatric indications for PAXOTIN-CR-FORTE:
Key contraindications and monitoring requirements:
Dellwich Lifescience LLP is an established pharmaceutical company based in Science City, Ahmedabad, Gujarat, dedicated to advanced formulation technology, uncompromising quality assurance, and ethical healthcare supply. Through our specialized neurology division, Blessme, we manufacture and market superior neuro-psychiatric treatments, including PAXOTIN-CR-FORTE (Paroxetine CR 25 mg + Clonazepam 0.5 mg Tablets).
We support PCD pharma franchise partners, hospital supply chains, and contract manufacturing clients across India with guaranteed supply security, validated product dossiers, and prompt dispatch.
Whether you are seeking PAXOTIN-CR-FORTE for district monopoly PCD franchise distribution, third-party contract manufacturing, or hospital bulk procurement, Dellwich Lifescience LLP delivers dependable supply and competitive trade margins.
Secure district-level monopoly marketing rights for PAXOTIN-CR-FORTE and the complete Blessme neuropsychiatry range with visual aids, product glossaries, and promotional input support.
Turnkey manufacturing solutions for pharmaceutical marketing companies with flexible batch runs, rapid production turnaround, and full regulatory dossier support from Ahmedabad.
Direct bulk pharmaceutical supply agreements for multispecialty hospital chains, psychiatric nursing homes, and institutional medical tenders with prompt pan-India logistics.
When sourcing Paroxetine CR 25 mg Clonazepam tablets in India, PAXOTIN-CR-FORTE by Blessme provides exceptional clinical efficacy, reliable blister packaging, and comprehensive B2B franchise support.
Manufactured in accredited facilities using IP grade APIs, ensuring exact active content uniformity and controlled dissolution.
Tamper-evident, moisture-resistant aluminium strips protect tablets from ambient humidity and transport friction.
Direct factory dispatch with GST invoicing, verified batch COA, and dependable logistics coverage across all Indian states.
Exclusive district-level franchise rights for PAXOTIN-CR-FORTE and the Blessme portfolio with promotional visual aids.
Certificates of Analysis (COA), stability testing data, and MSDS readily available for institutional audits and tenders.
Direct access to Dellwich Lifescience product specialists for quick quotes, customized bulk orders, and customer assistance.
Authoritative answers to clinical, commercial, dosage, and regulatory questions regarding Paroxetine CR 25 mg + Clonazepam tablets.
PAXOTIN-CR-FORTE is a full-strength controlled-release oral prescription tablet from the Blessme division of Dellwich Lifescience. It contains Paroxetine Hydrochloride IP equivalent to Paroxetine 25 mg (controlled release) and Clonazepam IP 0.5 mg, formulated for severe refractory depression comorbid with acute panic attacks and severe anxiety.
PAXOTIN-CR-FORTE contains 25 mg Paroxetine CR (compared to 12.5 mg in PAXOTIN-CR-PLUS). It is prescribed when the patient requires full therapeutic maintenance dosing for severe major depressive disorder, refractory panic disorder with agoraphobia, or severe obsessive-compulsive symptoms.
Paroxetine 25 mg provides potent 24-hour SERT inhibition, restoring core neuroplasticity, mood vitality, and emotional stability over 2 to 4 weeks. Simultaneously, Clonazepam 0.5 mg provides immediate positive GABAergic limbic suppression, aborting acute panic attacks and autonomic anxiety surges from day one.
Psychiatrists typically advise taking PAXOTIN-CR-FORTE once daily, preferably in the morning with breakfast or at bedtime if Clonazepam-induced sedation is noticeable. Always swallow the tablet whole with water.
No. PAXOTIN-CR-FORTE must be swallowed whole. Crushing, splitting, or chewing ruptures the enteric polymer barrier, leading to rapid dose dumping of 25 mg Paroxetine, which can cause severe nausea, vomiting, and loss of 24-hour controlled efficacy.
Yes. Due to the Clonazepam 0.5 mg component, mild-to-moderate sedation, drowsiness, or lightheadedness can occur, particularly during initial days of therapy. Patients should avoid driving or operating heavy machinery until individual tolerance is established.
No. Abrupt stoppage can precipitate severe discontinuation reactions (dizziness, electric shock sensations, sensory disturbances, insomnia, and rebound panic). Gradual dose tapering under psychiatric direction is mandatory.
Alcohol is strictly prohibited. Combining alcohol with Paroxetine and Clonazepam can cause dangerous central nervous system depression, extreme sedation, respiratory suppression, and memory blackouts.
The Clonazepam component belongs to the benzodiazepine class and carries potential for dependence and tolerance when taken continuously over long periods. Clinicians typically re-evaluate the patient periodically to assess tapering strategies.
Use during pregnancy is contraindicated unless specifically evaluated and determined to be vital by a medical specialist, as both Paroxetine and Clonazepam can pose risks to the developing fetus.
PAXOTIN-CR-FORTE is supplied in premium 10x10 aluminium-aluminium foil strips (100 tablets per box) manufactured with high-barrier foil to guarantee extended shelf life across all Indian climate conditions.
Pharmaceutical distributors and stockists can submit an enquiry through our online form below or contact our neuropsychiatry franchise desk at +91 99099 31992 for monopoly territory allocation.
Yes. Dellwich Lifescience provides turnkey contract manufacturing for Paroxetine CR + Clonazepam tablets with WHO-GMP certification, customized branding, and on-time shipment dispatch from Ahmedabad.
Dellwich Lifescience LLP is headquartered on Science City Road, Ahmedabad, Gujarat, India, with rapid logistics connections across all Indian states.
Connect directly with Dellwich Lifescience LLP for trade pricing, district monopoly PCD rights, third-party manufacturing, or institutional hospital tender supplies.
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