NDC Code(s) : 55154-4450-8
Packager : Cardinal Health

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Norepinephrine bitartrateNorepinephrine bitartrate INJECTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-4450(NDC:36000-162)
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NOREPINEPHRINE BITARTRATE(UNII: IFY5PE3ZRW)
(NOREPINEPHRINE - UNII:X4W3ENH1CV) 		NOREPINEPHRINE1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE(UNII: 451W47IQ8X)
NITROGEN(UNII: N762921K75)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55154-4450-81 in 1 BAG 04/01/2012
14 mL in 1 AMPULE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040859 04/01/2012 10/31/2018

PRINCIPAL DISPLAY PANEL

Norepinephrine Bitartrate Injection, USP

4 mg/4 ml (1 mg per mL)

1 x 4 mL Ampule

bag label