Naltrexone Hydrochloride USP (Anhydrous) For Compounding (API)

Naltrexone Hydrochloride USP is an opioid antagonist medication that is used to treat opioid addiction and alcohol dependence. It works by blocking the effects of opioids and reducing the cravings for alcohol, making it easier for individuals to remain sober. It is a synthetic substance that can be used as an active pharmaceutical ingredient (API) in various medications. It is a white, crystalline powder that is soluble in water and has a molecular formula of C20H23NO4•HCl. The USP stands for United States Pharmacopeia, which sets the standards for drugs and healthcare products in the United States.

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Naltrexone Hydrochloride USP is a pharmaceutical ingredient used in compounding to treat alcohol and opioid dependence. It acts by blocking the effects of alcohol and opioids within the brain, reducing the cravings for these substances and helping individuals stay sober. During compounding, Naltrexone Hydrochloride may be combined with other medications or used in a customized dosage form to suit the patient’s individual needs. It is also available in tablet form for standard use.

Physical State: Solid
Description: White to almost white powder
Odor: Almost odorless
Flammability: May be combustible at high temperature
Solubility: Very soluble in water; slightly soluble in alcohol; practically insoluble in dichloromethane and methylene chloride
pH: 4.5 - 6.0 (1%)
Conditions to avoid: Moisture, sunlight and extreme temperatures. Hygroscopic - Avoid exposure to moisture
Chemical Stability: Stable under recommended storage conditions. Store in original container, tightly sealed, protected from direct sunlight and moisture

CAS Number: 12650-69-0

Property: Light Sensitive