Product image of Neluptin (Tianeptine Sodium) supplied by GNH India

Neluptin

Active Ingredient:
Tianeptine Sodium
Origin:
EU

Neluptin (Tianeptine Sodium)

Tianeptine Sodium, the active ingredient in Neluptin, is an atypical antidepressant presented as an oral formulation for systemic use. It is indicated for the treatment of major depressive disorder in adult patients, helping to improve mood and functional capacity.

GNH India supplies Neluptin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for each batch. Customers benefit from reliable logistics, temperature‑controlled shipping where required, and responsive technical support throughout the procurement process.

Manufacturer / TM Owner

Lupin Europe Gmbh

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Indications & Clinical Uses

Tianeptine Sodium is employed in the management of depressive disorders and related conditions.

  • Major depressive disorder: reduces depressive symptoms and improves overall mood in adult patients.
  • Dysthymic disorder: provides sustained relief of chronic low‑grade depressive mood.
  • Anxiety associated with depression: alleviates anxiety symptoms that coexist with depressive episodes.

How It Works

  • Tianeptine Sodium exerts its antidepressant effect primarily by enhancing the reuptake of serotonin, thereby normalizing serotonergic transmission. In addition, it modulates glutamatergic neurotransmission through regulation of NMDA‑receptor activity and downstream signaling pathways, which contributes to neuroplasticity and stress‑response adaptation. The drug also influences the hypothalamic‑pituitary‑adrenal axis, reducing cortisol hypersecretion observed in depression.

Side Effects

Tianeptine Sodium may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Dry mouth: reduced salivary flow.
  • Constipation: decreased bowel movements.
  • Dizziness: sensation of light‑headedness.
  • Insomnia: difficulty initiating or maintaining sleep.

Serious or Rare Side Effects

  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Serotonin syndrome: agitation, hyperthermia, and neuromuscular abnormalities.
  • Suicidal thoughts: emergence or worsening of suicidal ideation.
  • Seizures: convulsive episodes.
  • Cardiovascular events: arrhythmia or myocardial infarction.

Precautions & Warnings

When prescribing Tianeptine Sodium, clinicians should consider several precautionary measures to ensure safe use.

  • Hepatic assessment: evaluate liver function before initiating therapy.
  • Mood monitoring: observe for worsening depression or emergence of suicidal thoughts.
  • Discontinuation: avoid abrupt cessation to reduce risk of withdrawal symptoms.
  • Substance misuse: use with caution in patients with a history of drug dependence.
  • Concomitant CNS depressants: monitor for additive sedation.
  • Pregnancy and lactation: assess risk‑benefit ratio as safety data are limited.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Tianeptine Sodium can interact with other medicines; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe serotonin‑related toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs) or other serotonergic agents: potential for serotonin syndrome.
  • Alcohol: may enhance central nervous system depression.
  • Benzodiazepines: increased sedative effect.
  • Opioids: heightened risk of respiratory depression.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): possible alteration of bleeding risk.
  • CYP450 substrates (e.g., CYP2D6 metabolized drugs): may affect plasma concentrations.
  • Antihypertensives: additive blood pressure lowering.
  • Anticonvulsants: potential impact on seizure threshold.
  • Herbal supplements (e.g., St. John’s wort): may modify serotonergic activity.

Frequently Asked Questions

Nelupin contains Tianeptine Sodium, which is indicated for the treatment of major depressive disorder in adult patients. It helps to alleviate depressive symptoms and improve overall mood and functional capacity.

Tianeptine Sodium enhances serotonin reuptake, normalising serotonergic transmission, and modulates glutamatergic pathways through NMDA‑receptor regulation. These actions promote neuroplasticity and reduce stress‑related neurochemical imbalances, contributing to its antidepressant effect.

The appropriate dose of Neluptin is determined by the prescribing clinician based on the individual patient's condition, response, and tolerability. Dosage regimens are not disclosed here and should follow the prescriber’s instructions.

Safety data for Tianeptine Sodium in pregnancy and lactation are limited. Clinicians should weigh potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing individuals.

To order, submit an enquiry on the Neluptin product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Unlike selective serotonin reuptake inhibitors, Tianeptine Sodium enhances serotonin reuptake and also modulates glutamatergic neurotransmission. This distinct mechanism may offer benefits for patients who do not respond adequately to SSRIs, though clinical choice depends on individual response and tolerability.

Nelupin should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain stability.

Nelupin is formulated for oral administration. Patients should swallow the tablet or capsule with water as directed by their healthcare professional, typically with or without food according to the prescriber’s guidance.

Serious adverse events include hepatic dysfunction, severe allergic reactions such as anaphylaxis, serotonin syndrome, emergence of suicidal thoughts, seizures, and cardiovascular complications like arrhythmia or myocardial infarction. Prompt medical attention is required if any of these occur.

Nelupin is contraindicated in patients with known hypersensitivity to Tianeptine Sodium or any excipients, and in individuals currently taking monoamine oxidase inhibitors. Caution is advised for those with severe liver disease, uncontrolled hypertension, or a history of substance misuse.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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