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|Product Name:||Prilocaine||Appearance:||White To Pale Yellow Crystalline Powder|
Local Anesthetic Agents,
Injectable Local Anesthetics
High Quality Local Anesthetic Prilocaine Hydrochloride / Prilocaine HCl CAS: 1786-81-8 For Pain Relief
Shelf Life: 36 months
Applications: Pharmaceutical fields
Storage: Store in sealed containers at cool & dry place. Keep away from light, moisture, pest infestation.
Prilocaine is a local anesthetic of the amino amide type first prepared by Claes Tegner and Nils Löfgren. In its injectable form (trade name Citanest), it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used for intravenous regional anaesthesia (IVRA).
Relieving pain of normal intact skin and numbing skin to pain from injections and other medical procedures. Prilocaine cream is a local anesthetic. It works by blocking nerves from transmitting painful impulses to the brain
Prilocaine Hydrochloride Injection, USP, 4% is a sterile, non pyrogenic isotonic solution that contains a local anesthetic agent and is administered parenterally by injection. See INDICATIONS AND USAGE for specific uses.
Prilocaine cream is a eutectic mixture of lidocaine 2.5% and prilocaine 2.5% formulated as an oil in water emulsion. In this eutectic mixture, both anesthetics are liquid at room temperature and the penetration and subsequent systemic absorption of both prilocaine and lidocaine are enhanced over that which would be seen if each component in crystalline form was applied separately as a 2.5% topical cream.
|Description||Almost white powder||White or almost white powder|
|Solubility||Complies||Very soluble in alcohol and in acetone; Slightly soluble in water.|
|Identification||Complies||By IR comma; To match with the working standard|
|Residue on ignition||0.05percnt;||≤0.1percnt;|
|Related compound A||Not detected||≤0.01%|
|Related compounds||Complies||Not more than 0.2percnt; Of any individual impurity|
|Complies||Not more than one impurity exceeds 0.1percnt;|
|0.13percnt;||Not more than 0.5% of total impurities|
|Residual solvents||Not detected|
|Not detected||Ethanol Not more than0.5%|
|Conclusion; Conforms to USP37|
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