CHROMIUM CHROMIC CHLORIDE
CHROMIUM CHROMIC CHLORIDE INJECTION, USP 40 mcg/10 mL (4 mcg/mL) 10 mL VIAL
Approved
Approval ID
953ad6e9-c066-6dc3-e053-2a95a90a9025
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2020
Manufacturers
FDA
HF Acquisition Co LLC, DBA HealthFirst
DUNS: 045657305
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
CHROMIUM CHROMIC CHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51662-1415
Application NumberNDA018961
Product Classification
M
Marketing Category
C73594
G
Generic Name
CHROMIUM CHROMIC CHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateFebruary 22, 2020
FDA Product Classification
INGREDIENTS (4)
CHROMIC CHLORIDEActive
Quantity: 4 ug in 1 mL
Code: KB1PCR9DMW
Classification: ACTIM
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT