Full-Strength Antidepressant-Anxiolytic Ratio
Each tablet contains Escitalopram 10 mg and Clonazepam 0.5 mg with strict active assay uniformity and rapid dissolution complying with Indian Pharmacopoeia standards.
ESICARE-PLUS is a full-strength oral neuropsychiatric formulation combining Escitalopram Oxalate IP equivalent to Escitalopram 10 mg with Clonazepam IP 0.5 mg by Blessme, Dellwich Lifescience LLP. Specifically indicated for severe major depressive disorder comorbid with debilitating panic attacks, severe agoraphobia, and intense psychic agitation, delivering immediate GABAergic tranquilization while establishing long-term serotonergic mood stabilization.

Detailed pharmaceutical specifications, active API monograph compliance, full-strength SSRI-GABA synergy, and 4x5x10 blister packaging details for ESICARE-PLUS.
ESICARE-PLUS provides 10 mg Escitalopram paired with 0.5 mg Clonazepam. Formulated for patients suffering from severe depression complicated by frequent panic attacks, intense somatic anxiety, and persistent insomnia.
In-depth pharmacological evaluation of Escitalopram 10 mg + Clonazepam 0.5 mg tablets, marketed as ESICARE-PLUS by Blessme (Dellwich Lifescience LLP). Covers acute panic termination, major depression treatment, and pharmaceutical supply across India.
ESICARE-PLUS is a full-strength oral neuropsychiatric formulation combining an allosteric selective serotonin reuptake inhibitor (Escitalopram 10 mg) with a high-affinity positive GABA_A modulator (Clonazepam 0.5 mg).
When psychiatrists treat patients with severe major depression comorbid with panic attacks or acute suicidal anxiety, waiting 3 to 4 weeks for SSRI monotherapy is clinically precarious. ESICARE-PLUS bridges this critical gap by delivering immediate high-potency anxiolytic coverage from day one.
Approved neurological and psychiatric indications for ESICARE-PLUS include:
Escitalopram 10 mg selectively inhibits the serotonin transporter (SERT), preventing 5-HT reuptake and steadily increasing serotonergic tone 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.
Clinical criteria for selecting between the formulations:
ESICARE-PLUS must be taken strictly in accordance with medical advice:
ESICARE-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.
ESICARE-PLUS is manufactured in WHO-GMP certified facilities adhering to Schedule M protocols, ensuring micro-blend homogeneity and maximum packaging stability.
Each tablet contains Escitalopram 10 mg and Clonazepam 0.5 mg with strict active assay uniformity and rapid dissolution complying with Indian Pharmacopoeia standards.
Tamper-evident, tropicalized 4x5x10 blister strips prevent moisture ingress and light-induced degradation, ensuring active ingredient stability across diverse Indian climates.
Every batch is backed by authenticated Certificates of Analysis (COA), disintegration profiles, assay validation data, and Material Safety Data Sheets for hospital audits.
Produced in state-of-the-art accredited manufacturing units in Gujarat adhering to automated compression, online check-weighing, and Good Laboratory Practices (GLP).
Prescribing guidance, contraindications, and drug interactions for Escitalopram 10 mg + Clonazepam 0.5 mg tablets.
ESICARE-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 ESICARE-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 ESICARE-PLUS (Escitalopram 10 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 ESICARE-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 ESICARE-PLUS and the 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 Escitalopram Clonazepam tablets in India, ESICARE-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 fast disintegration.
Tamper-evident, moisture-resistant blister 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 ESICARE-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 Escitalopram + Clonazepam tablets.
ESICARE-PLUS is a full-strength oral prescription tablet from the Blessme division of Dellwich Lifescience. It contains Escitalopram Oxalate IP equivalent to Escitalopram 10 mg and Clonazepam IP 0.5 mg, formulated for severe depression comorbid with acute panic crises and psychiatric agitation.
ESICARE-PLUS contains 0.5 mg Clonazepam (compared to 0.25 mg in ESICARE-LS). It is chosen when the patient experiences severe panic disorder, intense somatic anxiety, severe sleep disturbances, or panic with agoraphobia requiring full-strength GABAergic limbic suppression.
Escitalopram 10 mg selectively inhibits the serotonin transporter (SERT), elevating synaptic 5-HT levels over 2 to 4 weeks to resolve core depressive symptoms. Concurrently, Clonazepam 0.5 mg acts immediately on GABA_A receptors, stimulating inhibitory chloride influx to provide prompt panic relief and anxiety suppression from day one.
Psychiatrists typically advise taking ESICARE-PLUS once daily. Because 0.5 mg Clonazepam can cause sedation, taking it at bedtime is frequently recommended to promote restorative sleep while protecting against nocturnal panic awakenings.
Yes. Due to the 0.5 mg Clonazepam content, mild-to-moderate sedation, drowsiness, or lightheadedness can occur, particularly during initial days of therapy. Patients should avoid driving, operating heavy machinery, or hazardous tasks until individual tolerance is established.
No. Abrupt stoppage can precipitate severe withdrawal symptoms (sensory disturbances, dizziness, rebound anxiety, 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 Escitalopram 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 evaluate the patient after 4 to 8 weeks to determine tapering strategies for the benzodiazepine.
Common side effects include drowsiness, fatigue, dry mouth, mild nausea, changes in appetite, or mild dizziness. Most side effects subside as the body adapts over the first two weeks of treatment.
Use during pregnancy is contraindicated unless specifically evaluated by a medical specialist, as both Escitalopram and Clonazepam can pose risks to the developing fetus.
ESICARE-PLUS is supplied in premium 4x5x10 blister strips (200 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 Escitalopram + Clonazepam combinations with GMP certification, customized branding, and on-time shipment dispatch.
Dellwich Lifescience LLP is headquartered on Science City Road, Ahmedabad, Gujarat, India, with rapid logistics connections across all Indian states.
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