COPPER
COPPER 0.4 mg/mL
Approved
Approval ID
a84d61a4-8e7f-4be1-aba6-f633b334aafc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 30, 2022
Manufacturers
FDA
Hospira, Inc.
DUNS: 141588017
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 Code0409-4092
Application NumberNDA018960
Product Classification
M
Marketing Category
C73594
G
Generic Name
CUPRIC CHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 30, 2022
FDA Product Classification
INGREDIENTS (5)
CUPRIC CHLORIDEActive
Quantity: 0.4 mg in 1 mL
Code: S2QG84156O
Classification: ACTIM
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT