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Lidocaine Base
Xylocaine

Lidocaine Base is used in topical formulations that rely on skin penetration

HUMAN API

Lidocaine Base

Lidocaine Base is a key Active Pharmaceutical Ingredient (API) belonging to the Amide-Type Local Anesthetics class. It is characterized by its rapid and extended efficacy in providing temporary local anesthesia and nerve blocks. Unlike its Hydrochloride salt (HCl), Lidocaine Base is primarily used in non-aqueous formulations and topical preparations (dermal and mucosal) where effective skin penetration is required.

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).
A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.
A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.
Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).
Therapeutic Class:
Local Anesthetic.
Mechanism of Action:
Inhibits voltage-gated sodium channels in neural membranes, thereby blocking the generation and conduction of nerve impulses, leading to localized anesthesia.
Clinical Application:
Topical anesthesia of the skin and mucous membranes, relief of hemorrhoidal pain and itching, and pain management prior to superficial medical procedures.
Competitive Advantage:
The Base form ensures superior absorption and penetration across intact tissues compared to the Hydrochloride salt, making it ideal for ointments and creams.
Ointments and Creams

Topical preparations for dermatology and surface anesthesia.

The base form, with its limited water solubility, ensures easy integration and stability within oily/fatty bases.

Suppositories

Anorectal and rectal formulations.

Excellent stability and compatibility with common suppository fatty bases.

Patches and Mucosal Films

Transdermal delivery systems.

The Lipophilic characteristics facilitate skin penetration for effective localized action.

Regulatory Compliance

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).

Certificate of Analysis (CoA)

A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.

Drug Master File (DMF)

A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.

Manufacturing Operations

Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).

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