Product image of Lamisilate (Terbinafine Hydrochloride) supplied by GNH India

Lamisilate

Active Ingredient:
Terbinafine Hydrochloride
Origin:
EU

Lamisilate (Terbinafine Hydrochloride)

Terbinafine Hydrochloride, the active ingredient in Lamisilate, is an allylamine antifungal presented as a topical formulation for skin use. It treats superficial fungal infections—including tinea pedis, tinea corporis, tinea cruris and tinea versicolor—and are commonly encountered in clinical practice.

GNH India supplies Lamisilate as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures consistent quality and regulatory compliance across EU and other markets. We adhere to stringent manufacturing standards and provide reliable supply chain support for healthcare providers.

Manufacturer / TM Owner

Karo Healthcare Ab

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Indications & Clinical Uses

Terbinafine Hydrochloride is an allylamine antifungal used to treat superficial dermatophyte infections.

  • Tinea pedis: reduces itching and clears fungal infection of the feet.
  • Tinea corporis: eliminates ring‑shaped lesions on the body.
  • Tinea cruris: resolves jock‑itch and clears fungal growth in the groin area.
  • Tinea versicolor: normalizes skin pigmentation by eradicating yeast overgrowth.

How It Works

  • Terbinafine Hydrochloride inhibits the fungal enzyme squalene epoxidase, blocking the conversion of squalene to ergosterol. This disruption impairs ergosterol synthesis, a critical component of fungal cell membranes, leading to accumulation of toxic squalene and ultimately causing fungal cell death without affecting human cells.

Side Effects

Terbinafine Hydrochloride may cause local skin reactions when applied topically.

Common Side Effects

  • Burning sensation at the application site.
  • Itching or pruritus.
  • Redness or erythema.
  • Dryness or flaking of the skin.
  • Mild irritation or stinging.
  • Contact dermatitis.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis).
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Extensive blistering or skin necrosis.
  • Systemic hypersensitivity with fever.
  • Rare hepatic toxicity.
  • Unexplained swelling of the face or throat.

Precautions & Warnings

Before using Lamisilate, consider the following precautions:

  • Assess for hypersensitivity: avoid use in patients with known allergy to terbinafine or related compounds.
  • Evaluate skin integrity: do not apply on open wounds or severely damaged skin.
  • Limit duration: follow prescriber instructions to prevent over‑use.
  • Monitor for systemic signs: discontinue if severe rash or systemic symptoms develop.
  • Pediatric use: ensure dosage form is appropriate for children as directed.
  • Store below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Terbinafine topical has limited systemic absorption, but potential interactions should be considered.

Major Interactions (Avoid)

  • Oral terbinafine: concurrent use may increase systemic exposure.
  • Strong CYP2D6 inhibitors: could raise terbinafine levels if absorbed.
  • Other topical antifungals containing the same active ingredient.

Moderate Interactions (Monitor Closely)

  • Alcohol‑based skin cleansers: may alter drug absorption.
  • Topical corticosteroids: may reduce antifungal efficacy.

Frequently Asked Questions

Lamisilate contains terbinafine hydrochloride and is indicated for the topical treatment of superficial fungal infections such as athlete’s foot (tinea pedis), ringworm (tinea corporis), jock itch (tinea cruris) and tinea versicolor. It works on the skin to eliminate the fungi responsible for these conditions.

Terbinafine hydrochloride blocks the fungal enzyme squalene epoxidase, preventing the synthesis of ergosterol, an essential component of fungal cell membranes. The resulting buildup of squalene and loss of ergosterol disrupts membrane integrity, leading to fungal cell death while sparing human cells.

The specific dosing regimen for Lamisilate is determined by the prescribing healthcare professional based on the infection type, severity, patient age and other clinical factors. Patients should follow the prescriber’s instructions and the product label for application frequency and duration.

Safety data for topical terbinafine during pregnancy or lactation are limited. The product should be used only if the potential benefit justifies any potential risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

To request Lamisilate, 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 and any necessary import documentation.

Lamisilate (topical terbinafine) belongs to the allylamine class, offering a fungicidal mechanism that differs from azole or polyene antifungals. It often provides faster symptom relief and a lower risk of resistance for dermatophyte infections compared with some azole creams, but choice of therapy should be guided by the prescriber.

Lamisilate should be stored below 25 °C in its original container, protected from moisture and direct light. Keeping the product in a cool, dry place helps maintain its stability and effectiveness throughout its shelf life.

Lamisilate is applied topically to the affected skin area, usually once or twice daily as directed by the prescriber. The skin should be clean and dry before application, and the medication should be spread thinly to cover the lesion and a small margin of surrounding skin.

While rare, serious adverse reactions can include severe allergic responses such as anaphylaxis, Stevens‑Johnson syndrome, toxic epidermal necrolysis, extensive blistering, or systemic hypersensitivity. Any signs of severe rash, swelling, or difficulty breathing require immediate medical attention.

Lamisilate should not be used by individuals with a known hypersensitivity to terbinafine, its salts, or any component of the formulation. It is also contraindicated on severely damaged or broken skin, and caution is advised in patients with a history of severe drug reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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