Active Ingredient: CUPRIC CHLORIDE
Proprietary Name: CUPRIC CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.4MG COPPER/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A212071
Product Number: 001
Approval Date: Oct 31, 2022
Applicant Holder Full Name: EXELA PHARMA SCIENCES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
