Delayed Intestinal Absorption
Polymer-coated matrix delays paroxetine release until passing through the stomach, significantly mitigating nausea and gastric irritation while ensuring 24h plasma stability.
PAXOTIN-CR-PLUS is an advanced controlled-release neuropsychiatric formulation combining Paroxetine Hydrochloride IP equivalent to Paroxetine 12.5 mg (CR) with Clonazepam IP 0.5 mg by Blessme, Dellwich Lifescience LLP. Specifically indicated for major depressive disorder comorbid with panic attacks, generalized anxiety, and social phobia, delivering immediate GABAergic tranquilization while establishing sustained 24-hour serotonergic restoration with superior gastric tolerability.

Detailed pharmaceutical specifications, active API monograph compliance, controlled-release matrix synergy, and 10x10 aluminium strip packaging details for PAXOTIN-CR-PLUS.
PAXOTIN-CR-PLUS provides 12.5 mg Paroxetine CR paired with 0.5 mg Clonazepam. Formulated for patients suffering from depression complicated by recurrent panic attacks, intense somatic anxiety, and panic with agoraphobia with reduced nausea.
In-depth pharmacological evaluation of Paroxetine CR 12.5 mg + Clonazepam 0.5 mg tablets, marketed as PAXOTIN-CR-PLUS by Blessme (Dellwich Lifescience LLP). Covers acute panic termination, depression treatment, and pharmaceutical supply across India.
PAXOTIN-CR-PLUS is a specialized oral neuropsychiatric formulation combining a controlled-release formulation of the selective serotonin reuptake inhibitor (Paroxetine CR 12.5 mg) with a high-affinity positive GABA_A modulator (Clonazepam 0.5 mg).
When psychiatrists initiate antidepressant therapy in patients with panic disorder or anxious depression, standard SSRIs can paradoxically aggravate jitteriness during the first 10 to 14 days. PAXOTIN-CR-PLUS bridges this critical vulnerability by delivering immediate high-potency anxiolytic coverage via Clonazepam while Paroxetine CR steadily upregulates neuroplastic mood resilience.
Approved neurological and psychiatric indications for PAXOTIN-CR-PLUS include:
Paroxetine is recognized as one of the most potent inhibitors of the serotonin transporter (SERT), preventing 5-HT reuptake and steadily increasing serotonergic neurotransmission in cortical and limbic synapses over a 2 to 4-week neuroplastic adaptation period.
Simultaneously, Clonazepam 0.5 mg acts as a high-potency positive allosteric modulator on the GABAA receptor-chloride ion channel 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.
Advantages of Paroxetine CR over Immediate-Release:
PAXOTIN-CR-PLUS must be taken strictly in accordance with medical advice:
PAXOTIN-CR-PLUS 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-PLUS is manufactured in WHO-GMP certified facilities adhering to Schedule M protocols, ensuring micro-blend homogeneity and maximum packaging stability.
Polymer-coated matrix delays paroxetine release until passing through the stomach, significantly mitigating nausea and gastric irritation while ensuring 24h plasma stability.
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 12.5 mg + Clonazepam 0.5 mg tablets.
PAXOTIN-CR-PLUS 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-PLUS:
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-PLUS (Paroxetine CR 12.5 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-PLUS 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-PLUS 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 Clonazepam tablets in India, PAXOTIN-CR-PLUS 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-PLUS 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 + Clonazepam tablets.
PAXOTIN-CR-PLUS is a controlled-release oral prescription tablet from the Blessme division of Dellwich Lifescience. It contains Paroxetine Hydrochloride IP equivalent to Paroxetine 12.5 mg (in controlled-release form) and Clonazepam IP 0.5 mg, formulated for major depression comorbid with acute panic attacks and severe anxiety.
Conventional immediate-release paroxetine dissolves rapidly in the stomach, which can cause significant nausea, dyspepsia, and gastric distress. Paroxetine CR uses a specialized enteric matrix that delays release until the tablet reaches the small intestine, providing a smooth 24-hour plasma curve with dramatically lower rates of nausea.
Paroxetine CR is one of the most potent selective serotonin reuptake inhibitors (SSRIs), elevating synaptic serotonin (5-HT) to resolve core depressive symptoms and obsessive worry over 2 to 4 weeks. Simultaneously, Clonazepam 0.5 mg acts immediately on GABA_A receptors to stimulate inhibitory chloride influx, terminating acute panic dread and somatic restlessness from day one.
Psychiatrists typically advise taking PAXOTIN-CR-PLUS once daily in the morning or at bedtime. It should be taken with or after meals. If daytime drowsiness is observed due to the 0.5 mg Clonazepam component, bedtime administration is frequently recommended.
No. PAXOTIN-CR-PLUS must be swallowed whole. Dividing, chewing, or crushing the tablet ruptures the controlled-release membrane, causing rapid drug release that can lead to acute side effects and loss of 24-hour therapeutic coverage.
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 withdrawal symptoms (sensory disturbances, dizziness, electric shock sensations, rebound panic, and insomnia) due to simultaneous cessation of the SSRI and benzodiazepine. 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 after 4 to 8 weeks to determine tapering strategies.
Use during pregnancy is contraindicated unless specifically evaluated and determined to be essential by a medical specialist, as both Paroxetine and Clonazepam can pose risks to the developing fetus.
PAXOTIN-CR-PLUS 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.
Get wholesale pricing, PCD franchise monopoly rights, and technical documentation for Paroxetine CR 12.5 mg + Clonazepam 0.5 mg Tablets.