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Lidocaine
HCl

To guarantee the highest purity and safety, we adhere to strict global standards

HUMAN API

Lidocaine HCL

Lidocaine Hydrochloride is a crucial salt form of the Amide-Type Local Anesthetics class, and it also serves as a Class IB Antiarrhythmic agent. This form is characterized by its high water solubility, making it the preferred Active Pharmaceutical Ingredient (API) for sterile injectable formulations and standard aqueous solutions.

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 and Class IB Antiarrhythmic Agent.
Mechanism of Action:
Inhibits fast voltage-gated sodium channels in nerve membranes and cardiac muscle cells, achieving local anesthesia and cardiac membrane stabilization..
Primary Clinical Application:
Injectable Anesthesia: Local infiltration, regional anesthesia, and nerve blocks. Cardiology: Treatment of acute ventricular arrhythmias.
Competitive Advantage:
Excellent water solubility and optimal stability characteristics in the sterile aqueous solutions required for injection.
Injectables

Sterile injectable solutions (2%, 1%, etc.) for medical and dental use.

Features high-grade sterility (often supplied in specific injectable grades) and rapid, complete solubility in water.

Topical Solutions/Sprays

Sprays, toners, and solutions for mucosal membranes.

Excellent stability in aqueous media, maintaining potency in mucosal anesthetic preparations.

Oral Formulations

Tablets or capsules (for antiarrhythmic use).

High-purity, standardized API powder for standard compression and filling processes.

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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