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FDA Approval

Heparin Sodium

Company

Cantrell Drug Company (DUNS: 035545763)

Effective Date

December 24, 2014

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Heparin(50 [USP'U] in 1 mL)

Products (1)

Heparin Sodium

NDC Product Code

52533-216

Route of Administration

INTRAVENOUS

Effective Date

December 24, 2014

Ingredients

Code: ZZ45AB24CAClass: ACTIMQuantity: 50 [USP'U] in 1 mL

Sodium ChlorideInactive

Code: 451W47IQ8XClass: IACTQuantity: 4.5 mg in 1 mL

WaterInactive

Code: 059QF0KO0RClass: IACT

Hydrochloric acidInactive

Code: QTT17582CBClass: CNTM

BENZYL ALCOHOLInactive

Code: LKG8494WBHClass: IACTQuantity: 0.0001 mL in 1 mL

Sodium hydroxideInactive

Code: 55X04QC32IClass: CNTM

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