Norepinephrine Bitartrate

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

Company

Cantrell Drug Company

DUNS: 035545763

Effective Date

March 6, 2015

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Norepinephrine(32 ug 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

52533-166

Route of Administration

INTRAVENOUS

Effective Date

March 6, 2015

Ingredients

Code: IFY5PE3ZRWClass: ACTIMQuantity: 32 ug in 1 mL

ANHYDROUS DEXTROSEInactive

Code: 5SL0G7R0OKClass: IACTQuantity: 50 mg in 1 mL

SODIUM CHLORIDEInactive

Code: 451W47IQ8XClass: IACTQuantity: 236.8 ug in 1 mL

SODIUM METABISULFITEInactive

Code: 4VON5FNS3CClass: IACTQuantity: 64 ug in 1 mL

WATERInactive

Code: 059QF0KO0RClass: IACT

Code: QTT17582CBClass: CNTM

Code: 55X04QC32IClass: CNTM