Product image of Metoclopramide Hydrochloride Noridem Enterprises (Metoclopramide Hydrochloride Monohydrate) supplied by GNH India

Metoclopramide Hydrochloride Noridem Enterprises

Active Ingredient:
Metoclopramide Hydrochloride Monohydrate
Origin:
EU

Metoclopramide Hydrochloride Noridem Enterprises (Metoclopramide Hydrochloride Monohydrate)

Metoclopramide Hydrochloride, the active ingredient in Metoclopramide Hydrochloride Noridem Enterprises, is a dopamine D2 receptor antagonist presented as an injectable solution for intramuscular and intravenous use. It is employed to control nausea and vomiting, to improve gastric emptying in gastroparesis, and to prevent postoperative and chemotherapy‑induced emesis in adult patients.

GNH India supplies Metoclopramide Hydrochloride Noridem Enterprises as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide through regulated distribution channels and adheres to EU quality standards, ensuring product integrity and traceability.

Manufacturer / TM Owner

Noridem Enterprises Ltd

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Indications & Clinical Uses

Metoclopramide Hydrochloride is used in the antiemetic and gastroprokinetic therapeutic area to manage disorders of nausea, vomiting and gastric motility.

  • Nausea and vomiting: reduces the frequency and intensity of acute and delayed emesis in adult patients.
  • Gastroparesis: accelerates gastric emptying, relieving symptoms such as early satiety and bloating.
  • Post‑operative nausea and vomiting (PONV): prevents or treats emesis following surgical procedures.
  • Chemotherapy‑induced nausea and vomiting (CINV): mitigates both acute and delayed nausea associated with cytotoxic therapy.

How It Works

  • Metoclopramide Hydrochloride blocks dopamine D2 receptors in the chemoreceptor trigger zone and throughout the gastrointestinal tract, diminishing the central stimulus for vomiting. It also antagonizes 5‑HT3 receptors and agonises 5‑HT4 receptors, which together enhance gastric motility and accelerate gastric emptying, thereby reducing nausea and vomiting.

Side Effects

Metoclopramide Hydrochloride may cause a range of adverse reactions.

Common Side Effects

  • Drowsiness: mild sedation or fatigue.
  • Restlessness: feelings of inner tension or akathisia.
  • Diarrhea: loose stools or increased bowel movements.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: dystonia, tremor, or rigidity.
  • Tardive dyskinesia: irreversible involuntary movements with long‑term use.
  • Neuroleptic malignant syndrome: rare but life‑threatening hyperthermia and muscle rigidity.
  • Severe allergic reactions: anaphylaxis, rash, or angioedema.
  • Hyperprolactinemia: galactorrhea or menstrual disturbances.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for known adverse effects.

  • Renal or hepatic impairment: adjust monitoring as drug clearance may be reduced.
  • Extrapyramidal risk: observe for signs of dystonia or tardive dyskinesia, especially with prolonged use.
  • Hypersensitivity: discontinue if allergic reactions occur.
  • Elderly patients: use caution due to increased susceptibility to sedation and falls.
  • Concomitant dopamine‑blocking agents: assess for additive effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Metoclopramide Hydrochloride can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • CNS depressants: may enhance sedation and respiratory depression.
  • Anticholinergic agents: increase risk of severe extrapyramidal reactions.
  • MAO inhibitors: potential for hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Opioids: may exacerbate reduced gastrointestinal motility.
  • SSRIs or other serotonergic drugs: raise the possibility of serotonin syndrome.
  • CYP2D6 inhibitors: can alter metoclopramide plasma levels, affecting efficacy and safety.

Frequently Asked Questions

Metoclopramide Hydrochloride is indicated for the treatment of nausea and vomiting, including postoperative and chemotherapy‑induced emesis, and for gastroparesis where it helps accelerate gastric emptying in adult patients.

The drug blocks dopamine D2 receptors in the brain’s chemoreceptor trigger zone and the gastrointestinal tract, reducing the vomiting reflex. It also antagonises 5‑HT3 receptors and stimulates 5‑HT4 receptors, which together promote gastric motility and improve stomach emptying.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s condition, age, weight, renal function and other clinical factors. Only a qualified healthcare professional should set the regimen.

Safety data for Metoclopramide Hydrochloride in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified prescriber.

To place an order, submit an enquiry on the 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 (including cold‑chain where required) and any necessary import documentation.

Metoclopramide is a dopamine D2 antagonist with additional 5‑HT3 antagonism and 5‑HT4 agonism, giving it both antiemetic and gastroprokinetic properties. Unlike pure 5‑HT3 antagonists (e.g., ondansetron), it also promotes gastric emptying, making it useful for gastroparesis, but it carries a higher risk of extrapyramidal side effects.

The injectable solution should be stored at 2‑8 °C (refrigerated), protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Metoclopramide Hydrochloride is supplied as an injectable solution for intramuscular or intravenous administration. The route, rate of infusion and dilution are determined by the prescribing clinician according to the indication and patient condition.

Serious risks include extrapyramidal reactions such as dystonia and tardive dyskinesia, neuroleptic malignant syndrome, severe allergic reactions (anaphylaxis), and hyperprolactinemia leading to galactorrhea or menstrual disturbances. Prompt medical attention is required if any of these occur.

Metoclopramide is contraindicated in patients with known hypersensitivity to the drug, in those with pheochromocytoma, and in individuals with a history of severe extrapyramidal reactions. Caution is also advised for patients with gastrointestinal obstruction, seizure disorders, or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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