ZINC
ZINC1 mg/mLZinc Chloride Injection, USP
Approved
Approval ID
9a1914a0-e195-4233-c1be-bc2075580eb8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 25, 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.
ZINC CHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0409-4090
Application NumberNDA018959
Product Classification
M
Marketing Category
C73594
G
Generic Name
ZINC CHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 25, 2021
FDA Product Classification
INGREDIENTS (4)
ZINC CHLORIDEActive
Quantity: 1 mg in 1 mL
Code: 86Q357L16B
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