CUPRIC CHLORIDE
CUPRIC CHLORIDE INJECTION, USP – solution
Approved
Approval ID
daaa6f3a-148e-4f1c-bd44-bb2242145b88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 16, 2019
Manufacturers
FDA
Exela Pharma Sciences, LLC
DUNS: 831274399
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
cupric chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51754-0103
Application NumberANDA212071
Product Classification
M
Marketing Category
C73584
G
Generic Name
cupric chloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 16, 2019
FDA Product Classification
INGREDIENTS (4)
CUPRIC CHLORIDEActive
Quantity: 0.4 mg in 1 mL
Code: S2QG84156O
Classification: ACTIM
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT