Regulatory PathRegulatory requirements compared

Active substance

Cupric

Open in the medicines table

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
CUPRIC CHLORIDE IN PLASTIC CONTAINEREQ 0.4MG COPPER/MLinjectable · injectionHOSPIRAPrescription26 Jun 1986
CUPRIC CHLORIDEEQ 0.4MG COPPER/MLinjectable · injectionEXELA PHARMAPrescription31 Oct 2022
CUPRIC SULFATEEQ 0.4MG COPPER/MLinjectable · injectionAM REGENTPrescription16 Dec 2022
CUPRIC CHLORIDEEQ 0.4MG COPPER/MLinjectable · injectionSOMERSETPrescription30 Apr 2024
CUPRIC CHLORIDEEQ 0.4MG COPPER/MLinjectable · injectionSTIRAPrescription30 Apr 2024
CUPRIC SULFATEEQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**injectable · injectionABRAXIS PHARMDiscontinued5 May 1987
CUPRIC SULFATEEQ 0.4MG COPPER/MLinjectable · injectionAPOTEX CORPDiscontinued19 Aug 2024
CUPRIC CHLORIDEEQ 0.4MG COPPER/MLinjectable · injectionAMNEALDiscontinued26 Jan 2026

Safety signals and safety-related labeling changes

All safety entries for cupric →

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.