Sodium Chromate 51

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 011038762

Effective Date

June 19, 2012

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Chromium Cr-51(1 mCi in 5 mL)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

AnazaoHealth Corporation

DUNS Number

011038762

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

51808-101

Route of Administration

INTRAVENOUS

Effective Date

October 13, 2012

Ingredients

SODIUM CHLORIDEInactive

Code: 451W47IQ8XClass: IACT

Code: 9QAU17N705Class: ACTIBQuantity: 1 mCi in 5 mL

BENZYL ALCOHOLInactive

Code: LKG8494WBHClass: IACTQuantity: 30 mg in 5 mL