Heparin Sodium

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

Company

Cantrell Drug Company

DUNS: 035545763

Effective Date

May 15, 2015

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Heparin(100 [USP'U] in 1 mL)

Products1

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

NDC Product Code

52533-179

Route of Administration

INTRAVENOUS

Effective Date

May 15, 2015

Ingredients

Code: ZZ45AB24CAClass: ACTIMQuantity: 100 [USP'U] in 1 mL

BENZYL ALCOHOLInactive

Code: LKG8494WBHClass: IACTQuantity: 0.0002 mL in 1 mL

WaterInactive

Code: 059QF0KO0RClass: IACT

Code: 55X04QC32IClass: CNTM

Code: QTT17582CBClass: CNTM

Sodium ChlorideInactive

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