Heparin Sodium
Heparin Sodium 25,000 USP Units Added to 0.45% Sodium Chloride 500 mL Bag
Approved
Approval ID
fda3f337-deab-40f3-bc0d-0c08baeb8a2d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 24, 2014
Manufacturers
FDA
Cantrell Drug Company
DUNS: 035545763
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Heparin Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52533-216
Product Classification
G
Generic Name
Heparin Sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 24, 2014
FDA Product Classification
INGREDIENTS (6)
Heparin SodiumActive
Quantity: 50 [USP'U] in 1 mL
Code: ZZ45AB24CA
Classification: ACTIM
Sodium ChlorideInactive
Quantity: 4.5 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: CNTM
BENZYL ALCOHOLInactive
Quantity: 0.0001 mL in 1 mL
Code: LKG8494WBH
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM