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terbinafine hydrochloride + lidocaine + glycyrrhizinate dipotassium + l-menthol

Cream 10 mg + 20 mg + 5 mg + 10 mg/g - 15 g

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
PICS
Manufacturer #17197

It is an integrated healthcare company founded in the 1920s. It has achieved top market value and sales revenue in the local pharmaceutical industry and has been awarded as the most respected and trusted company in East Asia for more than 10 years. The core business of the company can be classified into primary & specialty care, dietary supplements, household & animal care, and contract manufacturing of active pharmaceutical ingredients.

Manufacturer usually replies in 2 days

lidocaine + allantoin + tetrahydrozoline + chlorhexidine + l-menthol

Ointment 30 mg + 10 mg + 0.5 mg + 5 mg + 5 mg/g - 28 g

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
PICS
Comments
OTC
Manufacturer #17218
As a leading pharmaceutical company in Eastern Asia, the company has been dedicated and committed to the development and supply of superior pharmaceutical products that contribute to the health and well-being of people around the world. They have earned the trust of the companies with the ethical drugs franchise for chronic diseases, cancer therapies, antibiotics, and digestive and circulatory drugs.

Manufacturer usually replies in 11 days

l-menthol + camphor + methyl salicylate + chlorphenamine maleate + vanillyl nonylamide

Cutaneous solution 42 g + 4.5 g + 6.9 g + 0.1 g + 0.01 g - 45 ml, 90 ml, 120 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
FDA
Manufacturer #21263

​Established in 1959, this Manufacturer is a renowned CTD dossier owner and manufacturer based in Sejong, South Korea, with approximately 342 employees. As a GMP manufacturer, it specializes in producing over-the-counter (OTC) pharmaceutical products, including plasters, aerosols, topical liquids, emollients, hygiene products, ointments, adhesive bandages, mosquito repellents, anti-perspirants, cooling sheets, and bruise treatment creams. The Manufacturer's products are exported to approximately 30 countries worldwide. As a CTD dossier owner and manufacturer, it ensures compliance with international regulatory standards. Committed to excellence, this GMP manufacturer continues to expand its global presence, delivering high-quality healthcare solutions.​

Manufacturer usually replies in 30 days

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Terbinafine Hydrochloride Manufacturer

Terbinafine Hydrochloride is available under the brand name “Lamisil”. It belongs to the drug class of antifungal drugs. It is indicated for the treatment of skin infections which includes athlete’s foot, fungal nail infections, ringworm, jock itch, and pityriasis Versicolor. It can be administered through the oral route in the form of tablets or granules taken with soft food. Drugs that interact with this pharmaceutical medicine include warfarin, amiodarone, famotidine, rifampin, azole antifungals, tricyclic antidepressants, and many others. Only apply this medication topically. Make sure the treatment area is clean and dried completely before you begin. Once or twice daily, as instructed on the product label, apply a thin layer of the medication on and around the affected area. After use, wash your hands thoroughly unless the treatment area also includes your hands. Side effects associated with this pharmaceutical medicine include diarrhea, change or loss of smell and taste, vision changes, mental/mood changes, depression, bleeding/bruising, unusual tiredness, and kidney problems such as a change in urine frequency. It is contraindicated in conditions like depression, liver problems, systemic lupus erythematosus, abnormal liver function tests, and a drop in neutrophil count. It has been assigned as category B by the FDA. It is secreted in human milk in small amounts. If a 500mg oral dose is taken, only 0.65mg or 0.15mg will be excreted into milk which is 0.13% and 0.03% respectively. Its topical use on the breast should be avoided. It was approved by the FDA on 28th September 2007, under the brand name Lamisil manufactured by Novartis Pharmaceutical Corporation.

How does Terbinafine Hydrochloride work?

It has the fungicidal effect which is executed by inhibition of enzyme squalene monooxygenase, which in turn inhibits sterol biosynthesis of fungus by decreasing its ergosterol levels.

The cost of Terbinafine Hydrochloride

For a supply of 30 tablets of Terbinafine Hydrochloride oral tablets, 250mg it costs approximately $67.59.

Sourcing the Terbinafine Hydrochloride Manufacturer and Suppliers

Navigating our pharmaceutical marketplace

Being a global B2B pharmaceutical online marketplace, Pipelinepharma is designed to simplify pharmaceutical deals by providing you with an intuitive interface that is easy to engage with. The Terbinafine Hydrochloride manufacturers and suppliers can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. The advanced filters help you filter out the countries for this substance manufacturer and this substance supplier that you are looking for. These also enable you to check the dossier status of this medicine, and the GMP approvals of the different variants of Terbinafine Hydrochloride. Each manufacturer or supplier product description contains essential information about this substance including clinical data, stability zones, and countries. Manufacturers also have special delivery terms.

Establishing commercial ties

Pipelinepharma is a reliable B2B platform for prescription medicine sellers, wholesalers, and purchasers. Sellers that have a pharmaceutical permit can register and market an unlimited number of medications. sellers can interact and provide secondary services to customers directly instead of going through drug suppliers.

Quality assurance

During the registration process, Pipelinepharma assesses the data provided by the supplier. The site is used for product testing and evaluation. They must ensure that pharmaceutical medicines are free of flaws and that the duration of their usage is validated before they are sold as part of their obligations.

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