Norepinephrine Bitartrate
Norepinephrine Bitartrate 4 mg Added to 5% Dextrose 250 mL Bag
Approved
Approval ID
71f901b5-022b-43ea-b1a0-29adc9a1f718
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 6, 2015
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.
Norepinephrine Bitartrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52533-165
Product Classification
G
Generic Name
Norepinephrine Bitartrate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMarch 6, 2015
FDA Product Classification
INGREDIENTS (7)
ANHYDROUS DEXTROSEInactive
Quantity: 50 mg in 1 mL
Code: 5SL0G7R0OK
Classification: IACT
Norepinephrine BitartrateActive
Quantity: 16 ug in 1 mL
Code: IFY5PE3ZRW
Classification: ACTIM
SODIUM CHLORIDEInactive
Quantity: 118.4 ug in 1 mL
Code: 451W47IQ8X
Classification: IACT
SODIUM METABISULFITEInactive
Quantity: 32 ug in 1 mL
Code: 4VON5FNS3C
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: CNTM
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM