Chromium
CHROMIUMChromic ChlorideInjection, USP40 mcg/10 mL (4 mcg/mL)
Approved
Approval ID
da207ca8-7836-4c66-92fe-36cc89baf773
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 28, 2021
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.
Chromic Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-4093
Application NumberNDA018961
Product Classification
M
Marketing Category
C73594
G
Generic Name
Chromic Chloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 28, 2021
FDA Product Classification
INGREDIENTS (4)
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
CHROMIC CHLORIDEActive
Quantity: 4 ug in 1 mL
Code: KB1PCR9DMW
Classification: ACTIM
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT