MANGANESE
Manganese 0.1 mg/mL
Approved
Approval ID
6e979070-5035-4076-e09c-b52466be3c68
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 6, 2023
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.
MANGANESE CHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-4091
Application NumberNDA018962
Product Classification
M
Marketing Category
C73594
G
Generic Name
MANGANESE CHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 6, 2023
FDA Product Classification
INGREDIENTS (5)
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
MANGANESE CHLORIDEActive
Quantity: 0.1 mg in 1 mL
Code: QQE170PANO
Classification: ACTIM
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT