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NALTREXONE HYDROCHLORIDE USP (DIHYDRATE) (30-5086)



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A New Product from a World-Class Source 

 We now offer a dihydrate form of USP-grade naltrexone hydrochloride to meet the needs of your pharmacy and your patients. The manufacturer of PCCA Naltrexone Hydrochloride USP (Dihydrate) meets The PCCA Standard™ and has world-class qualifications: 

  • FDA registered
  • FDA inspected 
  • CGMP certified

Compounding with PCCA Naltrexone Hydrochloride USP (Dihydrate) 

Compounders need to refer to the certificate of analysis in order to calculate the correct amount of naltrexone hydrochloride on the anhydrous and solvent-free basis for their formulations. 

What is The PCCA Standard™? 

Our dihydrate naltrexone meets The PCCA Standard, which is our commitment to go above and beyond what is required to deliver the highest quality active ingredients, excipients and more for your compounding pharmacy. 

  • 850808-02-5
  • C20H23NO4*HCl*2H2O
  • 413.89
  • UN-Number:Not applicable (Not dangerous goods). UN proper shipping name:Not applicable (Not dangerous goods). Transport hazard class(es):Not applicable (Not dangerous goods). Packing group:Not applicable (Not dangerous goods). Environmental hazards:None. Special precautions for user:Not applicable. Transport in bulk according to Annex II of MARPOL73/78 and the IBC Code:Not applicable.

Caution: *PROTECT FROM LIGHT* *VERY HYGROSCOPIC* - For Prescription Compounding/Rx Only

Warning: Must be subjected to further processing during the preparation of injectable dosage forms to ensure acceptable levels of bacterial endotoxins.

Test Specification
DESCRIPTION WHITE OR ALMOST WHITE POWDER OR CRYSTALLINE POWDER
SOLUBILITY FREELY SOLUBLE IN WATER, SLIGHTLY SOLUBLE IN 96% ETHANOL