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FDA Approval

Glucoheptonate

CompanyAnazaoHealth Corporation (DUNS: 011038762)

Effective Date

May 23, 2012

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Calcium glucoheptonate(50 mg in 1 1)

Manufacturing Establishments (1)

AnazaoHealth Corporation

Labeler

AnazaoHealth Corporation

DUNS Number

011038762

Products (1)

Glucoheptonate

NDC Product Code

51808-213

Route of Administration

INTRAVENOUS

Effective Date

October 11, 2012

Ingredients

STANNOUS CHLORIDEInactive

Code: 1BQV3749L5Class: IACTQuantity: 0.6 mg in 1 1

Calcium glucoheptonateActive

Code: L11651398JClass: ACTIBQuantity: 50 mg in 1 1

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