Sodium Chromate 51
Sodium Chromate 51
Approved
Approval ID
0cc2c204-c14d-456b-b630-9e50d683a937
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 19, 2012
Manufacturers
FDA
AnazaoHealth Corporation
DUNS: 011038762
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Chromate 51
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51808-101
Product Classification
G
Generic Name
Sodium Chromate 51
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 13, 2012
FDA Product Classification
INGREDIENTS (3)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
CHROMIUM CR-51Active
Quantity: 1 mCi in 5 mL
Code: 9QAU17N705
Classification: ACTIB
BENZYL ALCOHOLInactive
Quantity: 30 mg in 5 mL
Code: LKG8494WBH
Classification: IACT